chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
11	36077761	36077762	G	A	13	GENIC	homozygous	126317968
11	36077889	36077890	T	C	20	GENIC	homozygous	115825376
11	36078061	36078062	T	C	25	GENIC	homozygous	115825378
11	36078203	36078204	T	C	9	GENIC	homozygous	115825382
11	36079457	36079458	G	A	17	GENIC	homozygous	115825386
11	36080566	36080567	G	A	10	GENIC	homozygous	115825390
11	36081013	36081014	C	A	20	GENIC	homozygous	126317969
11	36081594	36081595	A	G	22	GENIC	homozygous	115825394
11	36082757	36082758	A	C	14	GENIC	homozygous	115825398
11	36083096	36083097	A	G	30	GENIC	homozygous	115825402
11	36083574	36083575	G	A	3	GENIC	heterozygous	126317970
11	36086282	36086283	G	A	31	GENIC	homozygous	115825414
11	36086357	36086358	G	C	19	GENIC	homozygous	115825416
11	36086552	36086553	G	A	5	GENIC	homozygous	126317971
11	36088194	36088195	A	C	15	GENIC	homozygous	115825420
11	36088537	36088538	A	G	18	GENIC	homozygous	115825426
11	36088961	36088962	T	C	22	GENIC	homozygous	115825430
11	36089108	36089109	T	C	18	GENIC	homozygous	126317972
11	36089479	36089480	A	G	11	GENIC	homozygous	126317973
11	36089681	36089682	C	T	26	GENIC	homozygous	126317974
11	36089901	36089902	A	G	6	GENIC	homozygous	115825436
11	36091122	36091123	T	C	13	GENIC	homozygous	115962295
11	36091128	36091129	T	A	13	GENIC	homozygous	116038359
11	36091265	36091266	G	T	5	GENIC	heterozygous	126317975
11	36091370	36091371	T	C	14	GENIC	homozygous	115825449
11	36092195	36092196	G	C	11	GENIC	heterozygous	126272110
11	36092296	36092297	A	T	4	GENIC	homozygous	118143691