chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	190692946	190692946		A	33	GENIC	homozygous	135968605
2	190693273	190693274	T	C	43	GENIC	homozygous	136417114
2	190693274	190693275	C	T	43	GENIC	homozygous	136417115
2	190694807	190694808	A	G	51	GENIC	homozygous	136417116
2	190696020	190696021	A	G	56	GENIC	homozygous	136417117
2	190696974	190696975	C	T	45	GENIC	homozygous	136417118
2	190698670	190698671	A		13	GENIC	homozygous	403033815
2	190698670	190698671	A	T	13	GENIC	heterozygous	403033816
2	190698672	190698673	A		13	GENIC	homozygous	403033817
2	190698672	190698673	A	T	13	GENIC	heterozygous	403033818
2	190698674	190698675	A		13	GENIC	homozygous	403033819
2	190698674	190698675	A	T	13	GENIC	heterozygous	403033820
2	190698676	190698677	A		13	GENIC	homozygous	403563249
2	190698676	190698677	A	T	13	GENIC	heterozygous	403563250
2	190698678	190698679	A		13	GENIC	homozygous	403563251
2	190698678	190698679	A	T	13	GENIC	heterozygous	403563252
2	190698717	190698718	G	T	26	GENIC	homozygous	136417119
2	190698721	190698721		GA	27	GENIC	homozygous	135968606
2	190699010	190699010		ATTTT	43	GENIC	homozygous	135968607
2	190699591	190699592	T	G	61	GENIC	possibly homozygous	136417120
2	190700047	190700048	T	G	62	GENIC	homozygous	136417121