chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	40951444	40951445	T	C	42	GENIC	homozygous	109479588
1	40952887	40952888	T	C	29	GENIC	homozygous	109479589
1	40954273	40954274	C	G	37	GENIC	homozygous	109479591
1	40954989	40954990	G	A	33	GENIC	homozygous	109479594
1	40956244	40956245	A	G	38	GENIC	homozygous	109479595
1	40958263	40958264	G	C	29	GENIC	homozygous	109479597
1	40958561	40958562	A	C	11	GENIC	homozygous	108090510
1	40958695	40958696	C	T	29	GENIC	homozygous	109479598
1	40961979	40961980	A	G	21	GENIC	homozygous	109479599
1	40964901	40964902	T	C	30	GENIC	homozygous	109479603
1	40965170	40965171	G	A	18	GENIC	homozygous	109479604
1	40971520	40971521	A	G	53	GENIC	homozygous	109479606
1	40981238	40981239	C	T	18	GENIC	homozygous	109479611
1	40963857	40963858	C	T	2	GENIC	homozygous	120884767