chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	17343549	17343550	A		11	GENIC	homozygous	131114807
12	17343897	17343898	C	T	21	GENIC	homozygous	115559958
12	17346189	17346190	A	G	28	GENIC	homozygous	115365085
12	17344191	17344192	G	T	22	GENIC	possibly homozygous	115365079
12	17344392	17344393	A	G	28	GENIC	homozygous	115365080
12	17344670	17344671	T	C	22	GENIC	homozygous	115365081
12	17344807	17344808	T	C	20	GENIC	homozygous	115365082
12	17345142	17345143	T	C	26	GENIC	homozygous	115365083
12	17345985	17345986	C	T	23	GENIC	homozygous	115365084
12	17346364	17346365	T	C	25	GENIC	homozygous	115273561
12	17347062	17347063	A	G	25	GENIC	homozygous	115273563
12	17348831	17348832	A	G	29	GENIC	homozygous	115365086
12	17349307	17349308	T	C	20	GENIC	homozygous	115273565
12	17350951	17350952	G	A	27	GENIC	homozygous	115365087
12	17351964	17351965	T	C	19	GENIC	homozygous	115365088
12	17353329	17353330	A	G	20	GENIC	homozygous	115273573
12	17354336	17354337	A	T	24	GENIC	homozygous	115273575
12	17354338	17354339	T	G	25	GENIC	homozygous	115273576
12	17354515	17354516	A	G	20	GENIC	homozygous	115273580
12	17356326	17356327	C	T	28	GENIC	homozygous	115273584
12	17346271	17346272	T	C	35	GENIC	homozygous	115421341
12	17357171	17357172	G	A	25	GENIC	homozygous	115365089
12	17357452	17357453	G	C	28	GENIC	homozygous	115273586
12	17357535	17357536	T	C	21	GENIC	homozygous	115273588
12	17349600	17349600		GCA	11	GENIC	homozygous	131720042
12	17350594	17350598	GCCT		26	GENIC	homozygous	128966557
12	17357982	17357984	AC		27	GENIC	homozygous	128966561
12	17351850	17351850		AT	23	GENIC	possibly homozygous	131490357
12	17355192	17355197	GTGGG		18	GENIC	homozygous	131490358