chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	109666101	109666102	G	T	11	GENIC	homozygous	116718981
10	109666133	109666134	T	C	11	GENIC	homozygous	116718983
10	109666391	109666392	C	T	17	GENIC	homozygous	116718987
10	109667230	109667231	C	G	35	GENIC	homozygous	116909640
10	109667406	109667407	A	G	19	GENIC	homozygous	116718989
10	109667435	109667436	C	A	26	GENIC	homozygous	117136836
10	109667691	109667692	C	G	28	GENIC	homozygous	116909643
10	109667928	109667929	C	T	19	GENIC	homozygous	116909644
10	109668514	109668515	T	C	24	GENIC	homozygous	116909647
10	109668573	109668574	G	A	18	GENIC	homozygous	116909648
10	109668678	109668679	T	G	16	GENIC	homozygous	116909649
10	109669026	109669027	C	T	11	GENIC	homozygous	116909650
10	109669365	109669366	C	T	20	GENIC	homozygous	116909652
10	109669824	109669825	C	G	18	GENIC	homozygous	116909653
10	109669839	109669840	C	T	17	GENIC	homozygous	116909654
10	109669857	109669858	G	A	16	GENIC	homozygous	116909655
10	109670591	109670592	C	T	17	GENIC	homozygous	116909656
10	109670696	109670697	A	G	14	GENIC	homozygous	116909657
10	109670836	109670837	A	G	17	GENIC	homozygous	116909658
10	109671091	109671092	C	A	10	GENIC	homozygous	116909659
10	109671163	109671164	G	A	20	GENIC	homozygous	116909660
10	109671846	109671847	C	T	22	GENIC	homozygous	116909661
10	109671847	109671848	A	G	23	GENIC	homozygous	116909662
10	109672473	109672474	C	T	13	GENIC	homozygous	116718993
10	109672584	109672585	G	A	27	GENIC	homozygous	116909664
10	109673077	109673078	A	G	9	GENIC	homozygous	116909666
10	109673412	109673413	A	G	10	GENIC	possibly homozygous	116909667
10	109673548	109673549	T	G	15	GENIC	homozygous	116909668
10	109673790	109673791	A	G	19	GENIC	homozygous	116909669
10	109674110	109674111	A	G	20	GENIC	homozygous	116718995
10	109673838	109673839	A	G	14	GENIC	homozygous	116909670