chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	110046617	110046618	T	C	23	GENIC	homozygous	116719451
10	110046708	110046709	A	T	25	GENIC	homozygous	116719453
10	110046859	110046860	T	G	19	GENIC	homozygous	116843146
10	110047084	110047085	C	A	25	GENIC	homozygous	116719455
10	110047085	110047086	T	A	25	GENIC	homozygous	116719457
10	110050352	110050353	C	G	26	GENIC	homozygous	116719459
10	110058509	110058510	G	A	32	GENIC	homozygous	116719471
10	110062191	110062192	A	G	33	GENIC	possibly homozygous	116719473
10	110062808	110062809	A	G	27	GENIC	possibly homozygous	116719475
10	110068088	110068089	A	G	24	GENIC	homozygous	116719477
10	110072299	110072300	A	G	30	GENIC	possibly homozygous	116719479
10	110073317	110073318	A	G	34	GENIC	homozygous	116719481
10	110081607	110081608	A	G	28	GENIC	possibly homozygous	116909835
10	110088269	110088270	T	A	29	GENIC	possibly homozygous	116719485
10	110091701	110091702	G	T	8	GENIC	homozygous	116719487
10	110092344	110092345	A	G	20	GENIC	possibly homozygous	116719489
10	110096195	110096196	C	T	14	GENIC	homozygous	116719493
10	110096485	110096486	G	T	34	GENIC	possibly homozygous	117035873
10	110100222	110100223	T	G	23	GENIC	homozygous	116719495
10	110107169	110107170	G	T	19	GENIC	homozygous	116843148
10	110107170	110107171	T	G	19	GENIC	homozygous	116843150
10	110110488	110110489	G	C	21	GENIC	homozygous	116719497