chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45760608	45760609	T	A	55	GENIC	homozygous	116877336
10	45761812	45761813	A		58	GENIC	homozygous	131092456
10	45764787	45764788	T	C	48	GENIC	homozygous	116584426
10	45766214	45766215	G	C	44	GENIC	homozygous	116584432
10	45766473	45766474	G	C	50	GENIC	homozygous	116584434
10	45766883	45766888	AAATA		42	GENIC	homozygous	131092457
10	45766924	45766925	A	C	37	GENIC	homozygous	116877338
10	45766953	45766954	A	G	43	GENIC	homozygous	116877340
10	45767038	45767039	C	T	43	GENIC	homozygous	116877342
10	45775131	45775136	GAGGT		50	GENIC	homozygous	128814034
10	45778896	45778897	C	T	42	GENIC	homozygous	116877344
10	45780337	45780338	C	T	36	GENIC	homozygous	116877346
10	45781562	45781563	C	T	61	GENIC	homozygous	116584456
10	45788402	45788402		TC	40	GENIC	homozygous	128814037
10	45791371	45791372	T	C	59	GENIC	possibly homozygous	116877348
10	45791386	45791386		A	54	GENIC	possibly homozygous	131092458
10	45791437	45791438	G	A	51	GENIC	homozygous	116877350
10	45792731	45792735	CACG		33	GENIC	heterozygous	132145258