chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	101206697	101206698	G	A	57	GENIC	heterozygous	115199557
13	101206745	101206746	G	A	52	GENIC	heterozygous	114654391
13	101206780	101206781	T	A	65	GENIC	heterozygous	114654392
13	101206811	101206812	G	A	56	GENIC	heterozygous	115032960
13	101206814	101206815	T	C	53	GENIC	heterozygous	118467498
13	101206820	101206821	T	C	55	GENIC	heterozygous	118467499
13	101247463	101247464	C	T	14	GENIC	heterozygous	118467500
13	101233095	101233096	A	C	44	GENIC	heterozygous	118536960
13	101259517	101259518	C	T	27	GENIC	homozygous	115032964
13	101259705	101259706	G	T	11	GENIC	homozygous	118467501
13	101261556	101261557	A	T	5	GENIC	homozygous	118506057
13	101261913	101261914	T	A	6	GENIC	homozygous	118467503
13	101262248	101262249	T	G	16	GENIC	homozygous	118467504
13	101262885	101262886	T	C	16	GENIC	homozygous	118467506
13	101262923	101262924	G	A	15	GENIC	homozygous	118467507
13	101259622	101259623	G	T	22	GENIC	homozygous	114437773
13	101264060	101264061	C	A	9	GENIC	homozygous	114437775
13	101276558	101276559	G	T	17	GENIC	homozygous	114437777
13	101276620	101276621	A	C	3	GENIC	homozygous	118536961
13	101276746	101276747	C	A	31	GENIC	heterozygous	118467508
13	101276753	101276754	T	C	29	GENIC	heterozygous	118467509
13	101276761	101276762	C	T	28	GENIC	heterozygous	118467510