chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	31187257	31187258	C	T	28	GENIC	possibly homozygous	115810702
11	31189442	31189443	G	T	22	GENIC	homozygous	115810704
11	31189490	31189491	T	C	20	GENIC	homozygous	115810706
11	31189935	31189936	T	C	28	GENIC	homozygous	115810708
11	31190038	31190039	G	A	32	GENIC	homozygous	115810710
11	31191498	31191499	A	G	26	GENIC	possibly homozygous	115810712
11	31191629	31191630	T	C	21	GENIC	homozygous	115810714
11	31191662	31191663	C	T	29	GENIC	possibly homozygous	115810716
11	31192578	31192579	G	A	25	GENIC	possibly homozygous	115810718
11	31193491	31193492	A	T	22	GENIC	homozygous	115810720
11	31193696	31193697	T	G	29	GENIC	possibly homozygous	115810722
11	31195143	31195144	A	G	30	GENIC	possibly homozygous	115810724
11	31197053	31197054	C	T	29	GENIC	possibly homozygous	115810726
11	31197695	31197696	C	T	33	GENIC	possibly homozygous	115810728
11	31197711	31197712	G	A	30	GENIC	possibly homozygous	115810730
11	31197733	31197734	G	A	23	GENIC	possibly homozygous	115810732
11	31197912	31197913	C	A	18	GENIC	homozygous	115810734
11	31198076	31198077	A	T	16	GENIC	homozygous	115810736
11	31200750	31200751	T	C	18	GENIC	homozygous	115810740
11	31201054	31201055	C	T	25	GENIC	possibly homozygous	115810742
11	31202898	31202899	G	A	32	GENIC	possibly homozygous	115810744
11	31203020	31203021	G	A	27	GENIC	possibly homozygous	115810746
11	31205102	31205103	G	A	30	GENIC	possibly homozygous	115810748
11	31208044	31208045	C	T	27	GENIC	possibly homozygous	115810750
11	31210124	31210125	C	G	28	GENIC	possibly homozygous	115810754
11	31210272	31210273	C	A	35	GENIC	possibly homozygous	115810756
11	31212230	31212231	A	T	24	GENIC	possibly homozygous	115810758
11	31212583	31212584	G	C	31	GENIC	possibly homozygous	115810760
11	31213109	31213110	C	T	21	GENIC	possibly homozygous	115810762
11	31209496	31209497	T	C	32	GENIC	homozygous	116129246