chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
9	10696027	10696028	A	G	68	GENIC	homozygous	138513691
9	10697809	10697810	C	T	68	GENIC	possibly homozygous	138513693
9	10697844	10697845	G	A	53	GENIC	homozygous	143404659
9	10698278	10698279	C	T	66	GENIC	possibly homozygous	143404660
9	10699579	10699580	G	C	57	GENIC	homozygous	143404661
9	10700286	10700287	C	G	65	GENIC	possibly homozygous	143404662
9	10701358	10701359	T	C	65	GENIC	homozygous	143404663
9	10701592	10701593	T	C	49	GENIC	homozygous	138513696
9	10701707	10701708	A	T	61	GENIC	homozygous	143404664
9	10701714	10701715	G	C	62	GENIC	homozygous	143404665
9	10702583	10702584	G	T	61	GENIC	homozygous	143404666
9	10703466	10703467	T	C	58	GENIC	homozygous	143404667
9	10704310	10704311	C	T	55	GENIC	homozygous	143404668
9	10707096	10707097	G	A	62	GENIC	homozygous	138513700
9	10707498	10707499	G	A	61	GENIC	homozygous	143404669
9	10707602	10707603	T	C	59	GENIC	homozygous	143404670
9	10708346	10708347	A	G	53	GENIC	homozygous	143404671
9	10708601	10708602	A	T	50	GENIC	homozygous	138513701
9	10709262	10709263	A	C	47	GENIC	homozygous	143404672
9	10709630	10709631	A	G	38	GENIC	homozygous	138513702
9	10709953	10709954	A	G	41	GENIC	homozygous	154569236
9	10710813	10710814	T	C	73	GENIC	homozygous	138513704
9	10711172	10711173	A	G	61	GENIC	possibly homozygous	143404673
9	10712380	10712381	T	C	77	GENIC	homozygous	138513705
9	10707218	10707218		G	33	GENIC	homozygous	143396586
9	10709936	10709940	TGGG		40	GENIC	homozygous	144052722
9	10698851	10698853	AA		47	GENIC	homozygous	143396584
9	10700125	10700125		A	66	GENIC	possibly homozygous	143396585
9	10699194	10699194		GTTATTTAA	45	GENIC	homozygous	138446567
9	10703142	10703143	T	C	83	GENIC	homozygous	149373534
9	10709932	10709933	G		37	GENIC	homozygous	144052721