chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	109643139	109643140	A	C	17	GENIC	homozygous	108175837
1	109643465	109643466	A	C	33	GENIC	homozygous	120564210
1	109643605	109643606	G	A	29	GENIC	homozygous	120870973
1	109644095	109644096	A	G	33	GENIC	homozygous	120564212
1	109644881	109644882	G	T	15	GENIC	homozygous	120564214
1	109645476	109645477	A	G	27	GENIC	homozygous	108913081
1	109645017	109645018	C	T	16	GENIC	homozygous	108913078
1	109645259	109645260	G	C	29	GENIC	homozygous	108913079
1	109645376	109645377	A	G	35	GENIC	homozygous	108913080
1	109645576	109645577	T	A	25	GENIC	homozygous	108913082
1	109645598	109645599	G	A	28	GENIC	homozygous	120564216
1	109646255	109646256	G	A	26	GENIC	homozygous	120564219
1	109647282	109647283	G	C	31	GENIC	homozygous	108913084
1	109647286	109647287	T	C	32	GENIC	homozygous	108175838
1	109647459	109647460	A	G	25	GENIC	homozygous	108913085
1	109647537	109647538	G	A	18	GENIC	homozygous	120564221
1	109648008	109648009	T	G	23	GENIC	homozygous	108913086
1	109648568	109648569	G	T	31	GENIC	homozygous	108913087
1	109648670	109648671	T	A	31	GENIC	homozygous	108913088
1	109648847	109648848	T	C	25	GENIC	homozygous	108913089
1	109648857	109648858	G	C	30	GENIC	homozygous	120564223
1	109649038	109649039	G	T	31	GENIC	homozygous	108913090
1	109649088	109649089	T	C	31	GENIC	homozygous	108913091
1	109649423	109649424	G	C	29	GENIC	homozygous	108913094
1	109649562	109649563	C	T	35	GENIC	homozygous	108913095
1	109649676	109649677	A	G	33	GENIC	homozygous	108913096