chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	93304593	93304594	A	T	40	GENIC	homozygous	116824687
10	93304649	93304650	A	G	32	GENIC	homozygous	116824689
10	93304751	93304752	T	C	18	GENIC	homozygous	116824691
10	93304767	93304768	T	C	20	GENIC	homozygous	116683394
10	93305176	93305177	G	A	25	GENIC	homozygous	116683398
10	93305261	93305262	C	T	27	GENIC	homozygous	116824693
10	93306113	93306114	C	T	45	GENIC	homozygous	116824695
10	93306478	93306479	C	A	23	GENIC	possibly homozygous	116906823
10	93306762	93306763	A	G	22	GENIC	homozygous	116683422
10	93306766	93306767	A	G	22	GENIC	homozygous	116683424
10	93306879	93306880	C	T	23	GENIC	homozygous	116824697
10	93306907	93306908	C	T	23	GENIC	homozygous	116824699
10	93307043	93307044	G	A	33	GENIC	homozygous	116824701
10	93308631	93308632	T	C	22	GENIC	homozygous	116824703
10	93309050	93309051	C	G	24	GENIC	homozygous	116824705
10	93310383	93310384	C	A	29	GENIC	homozygous	116824709
10	93310768	93310769	A	T	15	GENIC	heterozygous	116906824
10	93311060	93311061	A	G	22	GENIC	homozygous	116824711
10	93318043	93318044	A	G	22	GENIC	homozygous	116824715
10	93318287	93318288	A	C	30	GENIC	homozygous	116683496
10	93319092	93319093	T	C	21	GENIC	homozygous	116824717
10	93319452	93319453	T	C	15	GENIC	homozygous	116683498
10	93320755	93320756	T	A	24	GENIC	homozygous	116683500
10	93323519	93323520	A	T	28	GENIC	homozygous	116683506
10	93323548	93323549	C	A	33	GENIC	homozygous	116824719
10	93323752	93323753	G	A	31	GENIC	homozygous	116824721
10	93324840	93324841	A	C	13	GENIC	homozygous	116683508
10	93331265	93331266	G	A	12	GENIC	homozygous	116824723
10	93331667	93331668	T	C	24	GENIC	homozygous	116683512
10	93331990	93331991	A	G	29	GENIC	homozygous	116824725