ttype	patient	gene	classification	type	chr	pos	ref_allele	newbase	context65	cons46
BRCA	BR-0031	CTCF	DNP	Missense_Mutation	16	67662337	GC	CT	46	100
HNSC	HN_63021	CTCF	SNP	Missense	16	67660496	G	A	35	100
LUAD	LUAD-B02594	CTCF	SNP	Missense_Mutation	16	67644974	G	T	42	78
LUAD	LUAD-RT-S01810	CTCF	SNP	Silent	16	67654647	G	T	40	49
MEL	MEL-Ma-Mel-36	CTCF	SNP	Missense_Mutation	16	67654624	C	T	31	100
MM	MM-0421-FIX	CTCF	SNP	Synonymous	16	67650676	C	T	27	46
LUAD	TCGA-05-4395	CTCF	SNP	Silent	16	67645894	G	C	40	23
OV	TCGA-13-1497	CTCF	SNP	Missense_Mutation	16	67645945	G	C	33	63
LUSC	TCGA-18-3409	CTCF	SNP	Missense_Mutation	16	67662408	C	T	22	100
OV	TCGA-24-2035	CTCF	SNP	Synonymous	16	67663345	C	T	27	48
LUAD	TCGA-35-5375	CTCF	SNP	Missense_Mutation	16	67660607	G	A	38	85
LUAD	TCGA-44-2655	CTCF	SNP	Silent	16	67662413	G	T	39	43
LUAD	TCGA-44-2655	CTCF	SNP	Silent	16	67663408	C	T	28	44
LUAD	TCGA-44-3918	CTCF	SNP	Missense_Mutation	16	67654636	G	A	47	100
LUSC	TCGA-60-2698	CTCF	SNP	Silent	16	67671757	C	G	29	54
LUSC	TCGA-60-2726	CTCF	SNP	Silent	16	67645107	A	G	14	55
LUAD	TCGA-64-5781	CTCF	SNP	Splice_site	16	67670753	G	T	34	71
LUSC	TCGA-66-2786	CTCF	SNP	Silent	16	67662443	A	G	8	65
BRCA	TCGA-A2-A0CQ	CTCF	SNP	Missense_Mutation	16	67654645	C	G	30	100
BRCA	TCGA-A2-A0YF	CTCF	INS	Splice_Site	16	67645853	-	TAC	35	100
UCEC	TCGA-A5-A0GA	CTCF	SNP	Missense_Mutation	16	67654642	C	T	27	100
UCEC	TCGA-A5-A0GH	CTCF	DEL	Frame_Shift_Del	16	67645967	TG	-	55	91
UCEC	TCGA-A5-A0GI	CTCF	SNP	Nonsense_Mutation	16	67655479	C	T	23	63
UCEC	TCGA-A5-A0GM	CTCF	SNP	Nonsense_Mutation	16	67645291	C	T	21	74
UCEC	TCGA-A5-A0GM	CTCF	SNP	Splice_Site	16	67645517	G	A	44	100
UCEC	TCGA-A5-A0GP	CTCF	SNP	Nonsense_Mutation	16	67655479	C	T	23	63
UCEC	TCGA-A5-A0R9	CTCF	SNP	Missense_Mutation	16	67654646	C	T	23	100
UCEC	TCGA-A5-A0VO	CTCF	SNP	Nonsense_Mutation	16	67660616	C	T	17	100
CRC	TCGA-A6-2672	CTCF	SNP	Missense_Mutation	16	67663406	C	T	27	79
CRC	TCGA-A6-2676	CTCF	SNP	Missense_Mutation	16	67650719	C	T	31	99
BRCA	TCGA-A8-A0AD	CTCF	SNP	Missense_Mutation	16	67645922	C	T	29	99
CRC	TCGA-AA-3518	CTCF	SNP	Missense_Mutation	16	67662412	C	T	27	100
CRC	TCGA-AA-3667	CTCF	SNP	Missense_Mutation	16	67660607	G	T	38	85
CRC	TCGA-AA-3845	CTCF	SNP	Missense_Mutation	16	67660580	C	T	27	84
CRC	TCGA-AA-A00D	CTCF	SNP	Missense_Mutation	16	67644779	C	G	20	70
CRC	TCGA-AA-A010	CTCF	SNP	Missense_Mutation	16	67650729	A	G	6	90
AML	TCGA-AB-3009	CTCF	SNP	Nonsense_Mutation	16	67660469	C	T	27	58
CRC	TCGA-AG-A002	CTCF	SNP	Missense_Mutation	16	67650710	C	T	31	84
CRC	TCGA-AG-A026	CTCF	SNP	Missense_Mutation	16	67644806	C	G	20	94
BRCA	TCGA-AN-A0AT	CTCF	SNP	Nonsense_Mutation	16	67645308	G	A	42	100
BRCA	TCGA-AN-A0FS	CTCF	SNP	Missense_Mutation	16	67645507	A	G	13	92
BRCA	TCGA-AO-A12B	CTCF	DEL	Frame_Shift_Del	16	67644796	GAGA	-	41	94
UCEC	TCGA-AP-A051	CTCF	SNP	Missense_Mutation	16	67645223	G	A	43	100
UCEC	TCGA-AP-A059	CTCF	SNP	Missense_Mutation	16	67654607	A	C	1	94
UCEC	TCGA-AP-A059	CTCF	SNP	Silent	16	67660564	A	G	6	53
UCEC	TCGA-AP-A0LL	CTCF	INS	Frame_Shift_Ins	16	67670599	-	T	28	87
UCEC	TCGA-AP-A0LM	CTCF	SNP	Missense_Mutation	16	67670668	C	T	24	61
UCEC	TCGA-AP-A0LP	CTCF	SNP	Missense_Mutation	16	67654643	G	A	40	100
UCEC	TCGA-AX-A05T	CTCF	DEL	Frame_Shift_Del	16	67645502	AAATT	-	1	79
UCEC	TCGA-AX-A05Y	CTCF	SNP	Missense_Mutation	16	67654643	G	A	40	100
UCEC	TCGA-AX-A05Z	CTCF	SNP	Missense_Mutation	16	67645102	A	G	10	68
UCEC	TCGA-AX-A05Z	CTCF	SNP	Nonsense_Mutation	16	67645270	G	T	33	87
UCEC	TCGA-AX-A06H	CTCF	INS	Frame_Shift_Ins	16	67646012	-	AC	13	91
UCEC	TCGA-AX-A0J0	CTCF	SNP	Nonsense_Mutation	16	67645069	G	T	33	83
UCEC	TCGA-B5-A0JV	CTCF	SNP	Missense_Mutation	16	67662451	G	A	40	100
UCEC	TCGA-B5-A0K7	CTCF	SNP	Nonsense_Mutation	16	67662323	C	A	19	46
UCEC	TCGA-B5-A11R	CTCF	SNP	Nonsense_Mutation	16	67645273	C	T	17	100
UCEC	TCGA-B5-A11X	CTCF	DEL	Frame_Shift_Del	16	67644787	A	-	13	86
UCEC	TCGA-B5-A11Y	CTCF	SNP	Nonsense_Mutation	16	67655479	C	T	23	63
BRCA	TCGA-B6-A0RI	CTCF	SNP	Splice_Site	16	67645518	T	G	57	91
BRCA	TCGA-B6-A0WZ	CTCF	SNP	Missense_Mutation	16	67655464	G	C	45	100
KIRC	TCGA-B8-4151	CTCF	SNP	Missense_Mutation	16	67660544	C	A	24	100
HNSC	TCGA-BA-5151	CTCF	INS	Frame_Shift_Ins	16	67645241	-	G	59	92
UCEC	TCGA-BG-A0LX	CTCF	SNP	Nonsense_Mutation	16	67644949	C	T	29	94
UCEC	TCGA-BG-A0M4	CTCF	INS	Frame_Shift_Ins	16	67646012	-	AC	13	91
UCEC	TCGA-BG-A0M4	CTCF	SNP	Nonsense_Mutation	16	67655479	C	T	23	63
UCEC	TCGA-BG-A0M9	CTCF	SNP	Nonsense_Mutation	16	67645273	C	T	17	100
UCEC	TCGA-BG-A0MC	CTCF	SNP	Missense_Mutation	16	67654646	C	T	23	100
UCEC	TCGA-BG-A0MO	CTCF	DEL	Frame_Shift_Del	16	67670650	T	-	52	81
UCEC	TCGA-BG-A0MQ	CTCF	SNP	Missense_Mutation	16	67646007	A	G	6	90
UCEC	TCGA-BG-A0VV	CTCF	SNP	Nonsense_Mutation	16	67660469	C	T	27	58
UCEC	TCGA-BG-A186	CTCF	SNP	Missense_Mutation	16	67654642	C	T	27	100
BRCA	TCGA-BH-A0BP	CTCF	SNP	Silent	16	67644837	A	G	3	53
BRCA	TCGA-BH-A0DH	CTCF	SNP	Missense_Mutation	16	67645922	C	A	29	99
BRCA	TCGA-BH-A0W4	CTCF	SNP	Missense_Mutation	16	67645919	C	T	31	100
BRCA	TCGA-BH-A0W5	CTCF	SNP	Missense_Mutation	16	67645923	A	C	6	91
UCEC	TCGA-BK-A0C9	CTCF	SNP	Nonsense_Mutation	16	67645326	T	A	50	71
UCEC	TCGA-BK-A0C9	CTCF	SNP	Nonsense_Mutation	16	67645327	C	T	29	76
KIRC	TCGA-BP-4775	CTCF	SNP	Nonsense_Mutation	16	67644949	C	T	29	94
UCEC	TCGA-BS-A0T9	CTCF	SNP	Nonsense_Mutation	16	67655479	C	T	23	63
UCEC	TCGA-BS-A0T9	CTCF	SNP	Missense_Mutation	16	67662303	C	T	21	100
UCEC	TCGA-BS-A0U5	CTCF	SNP	Missense_Mutation	16	67650722	T	C	61	90
UCEC	TCGA-BS-A0UJ	CTCF	SNP	Missense_Mutation	16	67645354	A	C	2	76
UCEC	TCGA-BS-A0UM	CTCF	SNP	Nonsense_Mutation	16	67663367	G	T	33	79
UCEC	TCGA-BS-A0V6	CTCF	SNP	Nonsense_Mutation	16	67662338	C	A	27	58
BLCA	TCGA-BT-A0YX	CTCF	SNP	Silent	16	67662356	G	A	33	87
BLCA	TCGA-BT-A2LB	CTCF	SNP	Missense_Mutation	16	67650746	T	C	52	91
BRCA	TCGA-C8-A12T	CTCF	SNP	Nonsense_Mutation	16	67655431	G	T	33	100
BRCA	TCGA-C8-A134	CTCF	SNP	Silent	16	67645098	T	A	55	44
HNSC	TCGA-CQ-5327	CTCF	SNP	Missense_Mutation	16	67662366	C	G	32	87
HNSC	TCGA-CQ-5327	CTCF	SNP	Missense_Mutation	16	67662427	C	G	32	77
HNSC	TCGA-CQ-5334	CTCF	SNP	Silent	16	67650751	G	A	36	64
HNSC	TCGA-CQ-5334	CTCF	SNP	Nonsense_Mutation	16	67655479	C	T	23	63
HNSC	TCGA-CQ-6228	CTCF	SNP	Nonsense_Mutation	16	67670700	A	T	5	81
HNSC	TCGA-CR-7382	CTCF	SNP	Missense_Mutation	16	67650717	G	A	40	99
HNSC	TCGA-CV-6938	CTCF	SNP	Nonsense_Mutation	16	67670670	C	T	29	61
HNSC	TCGA-CV-7102	CTCF	SNP	Missense_Mutation	16	67660529	C	T	29	100
HNSC	TCGA-CV-7242	CTCF	SNP	Missense_Mutation	16	67660581	G	T	38	87
HNSC	TCGA-CV-7253	CTCF	SNP	Missense_Mutation	16	67650762	G	T	46	99
UCEC	TCGA-D1-A0ZR	CTCF	SNP	Splice_Site	16	67663300	G	C	33	94
UCEC	TCGA-D1-A0ZV	CTCF	SNP	Nonsense_Mutation	16	67645168	G	T	33	85
UCEC	TCGA-D1-A0ZV	CTCF	SNP	Missense_Mutation	16	67650756	C	T	30	99
UCEC	TCGA-D1-A161	CTCF	INS	Frame_Shift_Ins	16	67654681	-	GT	41	100
UCEC	TCGA-D1-A163	CTCF	SNP	Splice_site	16	67663303	T	A	49	50
UCEC	TCGA-D1-A163	CTCF	SNP	Missense_Mutation	16	67663337	C	A	22	65
UCEC	TCGA-D1-A16D	CTCF	INS	Frame_Shift_Ins	16	67650765	-	T	12	91
UCEC	TCGA-D1-A16Q	CTCF	SNP	Nonsense_Mutation	16	67655479	C	T	23	63
UCEC	TCGA-D1-A16X	CTCF	SNP	Missense_Mutation	16	67644740	A	G	9	71
UCEC	TCGA-D1-A16X	CTCF	SNP	Nonsense_Mutation	16	67670646	G	T	33	87
UCEC	TCGA-D1-A17D	CTCF	SNP	Missense_Mutation	16	67662298	G	A	38	100
UCEC	TCGA-D1-A17S	CTCF	SNP	Missense_Mutation	16	67654607	A	C	1	94
UCEC	TCGA-D1-A17U	CTCF	DEL	Frame_Shift_Del	16	67663409	T	-	54	72
BRCA	TCGA-D8-A1JC	CTCF	SNP	Silent	16	67662443	A	T	8	65
BRCA	TCGA-D8-A1X6	CTCF	SNP	Splice_site	16	67644736	A	G	4	71
BRCA	TCGA-E2-A156	CTCF	SNP	Nonsense_Mutation	16	67644796	G	T	41	94
BRCA	TCGA-E2-A15T	CTCF	SNP	Nonsense_Mutation	16	67670628	G	T	45	87
BRCA	TCGA-E2-A1L9	CTCF	DEL	Frame_Shift_Del	16	67644817	CGCCGGGAAGGGGG	-	19	71
BRCA	TCGA-E9-A1R0	CTCF	SNP	Missense_Mutation	16	67645418	T	C	64	92
BRCA	TCGA-E9-A227	CTCF	SNP	Missense_Mutation	16	67645934	C	G	21	99
BRCA	TCGA-EW-A1IY	CTCF	SNP	Missense_Mutation	16	67645412	A	G	14	92
BLCA	TCGA-FD-A3B3	CTCF	SNP	Silent	16	67662347	C	A	24	58
BLCA	TCGA-G2-A2EJ	CTCF	SNP	Missense_Mutation	16	67654676	G	A	34	100
HNSC	TCGA-H7-7774	CTCF	DEL	Frame_Shift_Del	16	67663349	GAGGGGGAAAATG	-	33	94
HNSC	TCGA-HL-7533	CTCF	SNP	Missense_Mutation	16	67670652	G	A	45	87
HNSC	TCGA-HL-7533	CTCF	SNP	Missense_Mutation	16	67671611	G	C	45	100