chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	10931614	10931615	G	T	22	GENIC	homozygous	109330614
20	10935058	10935059	C	G	27	GENIC	homozygous	109091686
20	10936563	10936564	A	G	30	GENIC	homozygous	109091688
20	10937915	10937916	A	G	20	GENIC	homozygous	109091690
20	10939109	10939110	T	G	7	GENIC	possibly homozygous	109422535
20	10939123	10939124	G	T	5	GENIC	heterozygous	109422537
20	10940250	10940251	T	G	27	GENIC	homozygous	109091692
20	10944968	10944969	C	T	20	GENIC	homozygous	109091696
20	10945744	10945745	C	T	21	GENIC	homozygous	109091698
20	10946827	10946828	C	T	37	GENIC	homozygous	109091700
20	10947664	10947665	C	T	22	GENIC	homozygous	109091702
20	10948331	10948332	C	T	49	GENIC	heterozygous	109422539
20	10948510	10948511	T	C	58	GENIC	heterozygous	109091704
20	10948516	10948517	C	T	59	GENIC	heterozygous	109091706
20	10948617	10948618	C	T	59	GENIC	heterozygous	109091710
20	10948618	10948619	T	A	61	GENIC	heterozygous	109091712
20	10948639	10948640	G	A	52	GENIC	heterozygous	109091716