chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	45760608	45760609	T	A	16	GENIC	homozygous	116877336
10	45761812	45761813	A		14	GENIC	homozygous	131092456
10	45764787	45764788	T	C	11	GENIC	homozygous	116584426
10	45766214	45766215	G	C	16	GENIC	homozygous	116584432
10	45766473	45766474	G	C	10	GENIC	homozygous	116584434
10	45766883	45766888	AAATA		9	GENIC	homozygous	131092457
10	45766924	45766925	A	C	12	GENIC	homozygous	116877338
10	45766953	45766954	A	G	11	GENIC	homozygous	116877340
10	45767038	45767039	C	T	11	GENIC	homozygous	116877342
10	45778896	45778897	C	T	15	GENIC	homozygous	116877344
10	45780337	45780338	C	T	15	GENIC	homozygous	116877346
10	45781562	45781563	C	T	16	GENIC	homozygous	116584456
10	45788402	45788402		TC	16	GENIC	homozygous	128814037
10	45775131	45775136	GAGGT		21	GENIC	homozygous	128814034
10	45791371	45791372	T	C	9	GENIC	homozygous	116877348
10	45791386	45791386		A	13	GENIC	homozygous	131092458
10	45791437	45791438	G	A	11	GENIC	homozygous	116877350