chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	94357527	94357529	GA		19	GENIC	homozygous	128847404
10	94357635	94357636	T	C	13	GENIC	homozygous	116685058
10	94358852	94358852		A	18	GENIC	homozygous	128847405
10	94360477	94360478	C	T	21	GENIC	homozygous	116685060
10	94360754	94360755	T	G	21	GENIC	possibly homozygous	116685062
10	94362196	94362197	A	T	20	GENIC	homozygous	116685064
10	94362307	94362308	C	G	18	GENIC	homozygous	116685066
10	94362617	94362618	T	G	23	GENIC	homozygous	116685068
10	94362891	94362891		A	20	GENIC	homozygous	128847406
10	94363088	94363089	A	G	20	GENIC	homozygous	116685070
10	94363481	94363482	A	G	19	GENIC	homozygous	116685072
10	94364509	94364510	T	C	22	GENIC	homozygous	116685074
10	94364856	94364857	C	T	19	GENIC	homozygous	116685076
10	94365055	94365056	A	T	19	GENIC	homozygous	116685078
10	94365827	94365828	G	A	26	GENIC	homozygous	116685080
10	94368125	94368126	G	A	15	GENIC	homozygous	116685082
10	94368384	94368385	G	C	19	GENIC	homozygous	116685084
10	94368547	94368548	G	A	17	GENIC	homozygous	116685086
10	94375951	94375952	A		25	GENIC	homozygous	128847407
10	94376942	94376943	T		17	GENIC	homozygous	128847408
10	94377276	94377277	G	A	27	GENIC	possibly homozygous	116685088
10	94381684	94381685	G	A	22	GENIC	homozygous	116685090