chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	17343549	17343550	A		22	GENIC	homozygous	131114807
12	17343897	17343898	C	T	12	GENIC	homozygous	115559958
12	17344191	17344192	G	T	18	GENIC	homozygous	115365079
12	17344392	17344393	A	G	22	GENIC	homozygous	115365080
12	17344670	17344671	T	C	21	GENIC	homozygous	115365081
12	17344807	17344808	T	C	25	GENIC	homozygous	115365082
12	17345142	17345143	T	C	22	GENIC	homozygous	115365083
12	17345985	17345986	C	T	24	GENIC	possibly homozygous	115365084
12	17346189	17346190	A	G	21	GENIC	homozygous	115365085
12	17346271	17346272	T	C	22	GENIC	homozygous	115421341
12	17346364	17346365	T	C	25	GENIC	homozygous	115273561
12	17347062	17347063	A	G	27	GENIC	homozygous	115273563
12	17348831	17348832	A	G	23	GENIC	homozygous	115365086
12	17349307	17349308	T	C	20	GENIC	homozygous	115273565
12	17349600	17349600		GCA	7	GENIC	homozygous	131720042
12	17350951	17350952	G	A	26	GENIC	homozygous	115365087
12	17351964	17351965	T	C	20	GENIC	homozygous	115365088
12	17353329	17353330	A	G	26	GENIC	homozygous	115273573
12	17354336	17354337	A	T	17	GENIC	homozygous	115273575
12	17354338	17354339	T	G	18	GENIC	homozygous	115273576
12	17354515	17354516	A	G	20	GENIC	homozygous	115273580
12	17355192	17355197	GTGGG		25	GENIC	homozygous	131490358
12	17356326	17356327	C	T	31	GENIC	homozygous	115273584
12	17357171	17357172	G	A	28	GENIC	homozygous	115365089
12	17357452	17357453	G	C	28	GENIC	homozygous	115273586
12	17357535	17357536	T	C	25	GENIC	homozygous	115273588
12	17350594	17350598	GCCT		27	GENIC	homozygous	128966557
12	17357982	17357984	AC		30	GENIC	homozygous	128966561