chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	104892541	104892542	G	A	16	GENIC	homozygous	116961622
10	104893892	104893893	A	G	25	GENIC	homozygous	116961624
10	104893959	104893960	A	G	17	GENIC	homozygous	116961626
10	104893991	104893992	T	C	15	GENIC	homozygous	116961628
10	104894068	104894069	G	A	27	GENIC	homozygous	116961630
10	104894101	104894102	G	A	33	GENIC	homozygous	116961632
10	104894234	104894235	T	G	24	GENIC	homozygous	116961634
10	104894390	104894391	T	C	24	GENIC	homozygous	116961636
10	104894634	104894635	A	G	34	GENIC	homozygous	116961638
10	104894996	104894997	A	T	14	GENIC	homozygous	116961640
10	104895016	104895017	A	G	10	GENIC	homozygous	116961642
10	104895188	104895189	C	T	19	GENIC	homozygous	116961644
10	104895231	104895232	G	T	18	GENIC	homozygous	116961646
10	104895414	104895415	A	G	25	GENIC	homozygous	116961648
10	104895624	104895625	A	C	20	GENIC	homozygous	116961650