chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	94166947	94166948	G	C	37	GENIC	homozygous	148272410
1	94167184	94167185	A	G	32	GENIC	homozygous	148272411
1	94167402	94167403	A	G	37	GENIC	homozygous	141219050
1	94167635	94167635		TTAG	30	GENIC	homozygous	141163360
1	94168398	94168399	A	G	43	GENIC	homozygous	148272412
1	94169177	94169178	T	C	32	GENIC	homozygous	141219052
1	94169294	94169294		AA	27	GENIC	homozygous	148263704
1	94170049	94170050	G	T	29	GENIC	homozygous	141219055
1	94170152	94170153	A	G	36	GENIC	homozygous	141219056
1	94170396	94170397	G	T	37	GENIC	homozygous	148272413
1	94171662	94171663	A	G	47	GENIC	homozygous	141219061
1	94172498	94172526	TGTGTGTATGTATGTATGTATGTATGTA		33	GENIC	possibly homozygous	148263705
1	94173248	94173249	A	G	29	GENIC	homozygous	141219063
1	94174272	94174273	C	A	45	GENIC	homozygous	141219066
1	94174640	94174641	A	G	41	GENIC	homozygous	141219067
1	94174965	94174966	G	A	44	GENIC	homozygous	141219068
1	94175063	94175064	C	A	35	GENIC	homozygous	141219069
1	94175079	94175080	A	G	37	GENIC	homozygous	141219070
1	94175179	94175180	G	C	46	GENIC	homozygous	141219071
1	94175595	94175596	C	T	28	GENIC	homozygous	148272414
1	94175953	94175954	T	G	33	GENIC	possibly homozygous	141219072
1	94176685	94176686	G	A	29	GENIC	homozygous	141219073
1	94176741	94176742	T	C	31	GENIC	homozygous	141219074
1	94176783	94176784	T	C	34	GENIC	homozygous	141219075
1	94176836	94176837	C	T	43	GENIC	homozygous	148272415
1	94172666	94172667	G		6	GENIC	heterozygous	402953050
1	94172715	94172716	C		6	GENIC	homozygous	403700080
1	94172715	94172716	C	T	6	GENIC	heterozygous	403700081
1	94172666	94172667	G	C	6	GENIC	homozygous	402953051