chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	9800322	9800323	T	C	48	GENIC	homozygous	111443653
3	9800532	9800533	T	G	44	GENIC	homozygous	111443654
3	9801166	9801167	C	T	44	GENIC	homozygous	111443655
3	9801301	9801302	A	C	44	GENIC	homozygous	111443656
3	9801844	9801845	A	G	33	GENIC	homozygous	111443657
3	9801879	9801880	T	C	37	GENIC	homozygous	111443658
3	9802434	9802435	T	C	21	GENIC	homozygous	111443659
3	9802850	9802851	C	A	33	GENIC	homozygous	111443660
3	9803225	9803226	A	G	46	GENIC	homozygous	111443661
3	9803771	9803772	A	G	38	GENIC	homozygous	111443663
3	9803819	9803820	A	G	43	GENIC	homozygous	111443664
3	9804295	9804296	A	G	22	GENIC	homozygous	111443667
3	9804615	9804616	G	A	49	GENIC	homozygous	119966890
3	9801768	9801769	C	T	34	GENIC	homozygous	119966888
3	9804493	9804494	G	A	37	GENIC	possibly homozygous	119966889
3	9803589	9803590	G	A	29	GENIC	homozygous	112223456
3	9804666	9804667	G	A	46	GENIC	homozygous	119966891
3	9805003	9805004	C	T	29	GENIC	homozygous	119966892
3	9805651	9805652	G	C	32	GENIC	homozygous	111443669
3	9806497	9806498	G	A	40	GENIC	homozygous	119966893
3	9807022	9807023	T	A	41	GENIC	homozygous	112330441
3	9807191	9807192	T	C	49	GENIC	homozygous	111443672