chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	83052590	83052591	T	G	38	GENIC	homozygous	50848654
11	83052616	83052617	T	C	28	GENIC	homozygous	50848655
11	83053528	83053529	T	C	33	GENIC	homozygous	50848656
11	83054822	83054823	A	AT	17	GENIC	possibly homozygous	50848657
11	83055415	83055416	C	T	20	GENIC	homozygous	50848658
11	83056956	83056958	AT	--	7	GENIC	heterozygous	50848659
11	83057119	83057120	C	G	17	GENIC	homozygous	50848660
11	83057437	83057438	C	T	22	GENIC	homozygous	50848661
11	83058568	83058569	C	CTA	9	GENIC	possibly homozygous	50848662
11	83058568	83058569	C	CTATA	9	GENIC	heterozygous	51025604
11	83060047	83060048	C	CTTAT	2	GENIC	homozygous	50848663
11	83061196	83061197	T	C	15	GENIC	homozygous	50848664
11	83061721	83061722	G	C	18	GENIC	homozygous	50848665
11	83062890	83062891	G	A	19	GENIC	homozygous	50848666
11	83064529	83064530	G	-	17	GENIC	homozygous	50848667
11	83064536	83064537	G	T	19	GENIC	homozygous	50848668
11	83064550	83064551	G	-	19	GENIC	homozygous	50848669
11	83064561	83064562	G	A	21	GENIC	homozygous	50848670
11	83064565	83064566	G	A	22	GENIC	homozygous	50848671
11	83064574	83064575	G	A	24	GENIC	homozygous	50848672
11	83064575	83064576	G	A	25	GENIC	homozygous	50848673
11	83064583	83064584	G	A	23	GENIC	homozygous	50848674
11	83064619	83064620	G	T	27	GENIC	homozygous	50848675
11	83066088	83066089	G	GA	21	GENIC	possibly homozygous	50848676
11	83066101	83066102	C	A	24	GENIC	homozygous	50848678
11	83066540	83066541	A	G	27	GENIC	homozygous	50848679
11	83068814	83068815	G	GT	18	GENIC	homozygous	50848680
11	83069179	83069180	G	GT	18	GENIC	possibly homozygous	50848681
11	83071328	83071329	G	GTTT	19	GENIC	homozygous	50848682
11	83059857	83059877	GAGAGAGAGAGAGAGAGAGA	--------------------	4	GENIC	homozygous	51191447
11	83064419	83064420	T	TATTCATAGTCATGCTGCCCTTCAGGCAATGTTAAAGTCATGCTGAACATGATGTAGCTTGAAAGC	25	GENIC	homozygous	51191448
11	83070526	83070530	TCTC	----	2	GENIC	heterozygous	51191449