chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	83052590	83052591	T	G	27	GENIC	homozygous	50848654
11	83052616	83052617	T	C	27	GENIC	homozygous	50848655
11	83053528	83053529	T	C	23	GENIC	homozygous	50848656
11	83054822	83054823	A	AT	17	GENIC	possibly homozygous	50848657
11	83055415	83055416	C	T	34	GENIC	homozygous	50848658
11	83056956	83056958	AT	--	5	GENIC	heterozygous	50848659
11	83057119	83057120	C	G	13	GENIC	homozygous	50848660
11	83057437	83057438	C	T	25	GENIC	homozygous	50848661
11	83058568	83058569	C	CTA	3	GENIC	homozygous	50848662
11	83060047	83060048	C	CTTAT	1	GENIC	homozygous	50848663
11	83061196	83061197	T	C	24	GENIC	homozygous	50848664
11	83061721	83061722	G	C	12	GENIC	homozygous	50848665
11	83062890	83062891	G	A	27	GENIC	homozygous	50848666
11	83064529	83064530	G	-	10	GENIC	homozygous	50848667
11	83064536	83064537	G	T	10	GENIC	homozygous	50848668
11	83064550	83064551	G	-	6	GENIC	homozygous	50848669
11	83064561	83064562	G	A	5	GENIC	homozygous	50848670
11	83064565	83064566	G	A	5	GENIC	homozygous	50848671
11	83064583	83064584	G	A	4	GENIC	homozygous	50848674
11	83064619	83064620	G	T	4	GENIC	homozygous	50848675
11	83066088	83066089	G	GA	26	GENIC	possibly homozygous	50848676
11	83066099	83066102	AAC	---	34	GENIC	heterozygous	50848677
11	83066101	83066102	C	A	37	GENIC	homozygous	50848678
11	83066540	83066541	A	G	40	GENIC	homozygous	50848679
11	83068814	83068815	G	GT	18	GENIC	homozygous	50848680
11	83069179	83069180	G	GT	16	GENIC	homozygous	50848681
11	83071328	83071329	G	GTTT	1	GENIC	homozygous	50848682