chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	36079218	36079219	C	T	29	GENIC	homozygous	51848958
10	36079343	36079344	A	G	17	GENIC	homozygous	51411305
10	36079630	36079631	A	G	19	GENIC	homozygous	51411307
10	36079697	36079698	A	G	27	GENIC	homozygous	51411309
10	36080066	36080067	A	G	23	GENIC	homozygous	51411313
10	36080119	36080120	G	C	24	GENIC	homozygous	51411315
10	36080290	36080291	C	G	29	GENIC	homozygous	51848962
10	36080573	36080574	A	G	23	GENIC	homozygous	51848965
10	36080959	36080960	T	C	33	GENIC	homozygous	51411321
10	36081655	36081656	A	AT	17	GENIC	homozygous	51848968
10	36084973	36084974	A	C	28	GENIC	homozygous	51411339
10	36085006	36085007	T	C	32	GENIC	homozygous	51411341
10	36086023	36086024	G	GCATA	14	GENIC	possibly homozygous	51848974
10	36086107	36086108	A	T	25	GENIC	homozygous	51411359
10	36086744	36086745	C	T	24	GENIC	possibly homozygous	51848976
10	36088695	36088696	T	C	33	GENIC	homozygous	51411391
10	36091763	36091764	A	G	33	GENIC	possibly homozygous	51411426
10	36091768	36091769	T	C	34	GENIC	possibly homozygous	52039185
10	36091947	36091948	G	A	22	GENIC	homozygous	52039187
10	36091995	36091996	A	AGCT	27	GENIC	homozygous	51411430
10	36092000	36092001	C	-	26	GENIC	homozygous	51411432
10	36092374	36092375	T	C	27	GENIC	homozygous	52039189
10	36092474	36092475	T	C	18	GENIC	homozygous	51411436
10	36092596	36092597	T	A	21	GENIC	homozygous	51411438
10	36092770	36092771	C	G	16	GENIC	homozygous	51411440
10	36092863	36092864	C	T	17	GENIC	homozygous	51411442
10	36092927	36092928	A	G	24	GENIC	homozygous	51411444
10	36092941	36092942	C	T	22	GENIC	homozygous	51411446
10	36093071	36093072	A	G	12	GENIC	homozygous	51411448
10	36093112	36093113	T	C	17	GENIC	possibly homozygous	51411450
10	36093765	36093766	T	A	26	GENIC	homozygous	51411452
10	36093850	36093851	C	G	36	GENIC	homozygous	51411454
10	36094012	36094013	G	T	38	GENIC	homozygous	51411456
10	36094178	36094187	CATCTGCAC	---------	34	GENIC	possibly homozygous	51411458