chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	89332176	89332177	C	T	18	GENIC	homozygous	117087428
10	89332819	89332820	C	T	24	GENIC	homozygous	116819859
10	89332981	89332982	T	C	24	GENIC	possibly homozygous	118048889
10	89333027	89333028	C	A	26	GENIC	possibly homozygous	118048890
10	89333476	89333477	G	T	27	GENIC	homozygous	116675240
10	89333255	89333256	G	A	17	GENIC	homozygous	116675234
10	89333345	89333346	T	C	20	GENIC	homozygous	116675236
10	89333640	89333641	G	A	25	GENIC	homozygous	117087430
10	89333707	89333708	A	T	30	GENIC	homozygous	116675242
10	89334047	89334048	T	C	24	GENIC	heterozygous	118048891
10	89334513	89334514	C	T	24	GENIC	homozygous	116675248
10	89334814	89334815	A	G	25	GENIC	homozygous	116675250
10	89335555	89335556	A	G	24	GENIC	homozygous	116675252
10	89335889	89335890	T	C	36	GENIC	homozygous	116675254
10	89336081	89336082	A	T	24	GENIC	homozygous	116675256
10	89336577	89336578	T	C	9	GENIC	homozygous	118048892
10	89337478	89337479	C	A	25	GENIC	homozygous	116675260
10	89337716	89337717	T	C	18	GENIC	homozygous	116675262
10	89338062	89338063	T	G	23	GENIC	homozygous	116675264
10	89337365	89337366	C	T	25	GENIC	homozygous	117068448
10	89333874	89333875	A	G	23	GENIC	homozygous	116950532
10	89336599	89336600	C	T	6	GENIC	homozygous	118117088