chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	87256491	87256492	G	A	19	GENIC	homozygous	117019513
10	87256560	87256561	A	G	25	GENIC	homozygous	116669640
10	87256721	87256722	G	A	18	GENIC	possibly homozygous	117019514
10	87256763	87256764	T	C	24	GENIC	possibly homozygous	117278974
10	87256824	87256825	G	A	23	GENIC	homozygous	117019515
10	87257410	87257411	C	T	29	GENIC	homozygous	117019516
10	87257906	87257907	T	C	36	GENIC	homozygous	116669642
10	87258108	87258109	C	T	33	GENIC	possibly homozygous	117019517
10	87258214	87258215	A	C	13	GENIC	heterozygous	117019518
10	87258608	87258609	T	C	34	GENIC	homozygous	116669646
10	87258609	87258610	G	T	33	GENIC	homozygous	117019519
10	87258836	87258837	T	C	24	GENIC	possibly homozygous	117019520
10	87259271	87259272	C	T	37	GENIC	possibly homozygous	117019521
10	87259703	87259704	A	G	22	GENIC	homozygous	116669650
10	87260298	87260299	A	G	29	GENIC	possibly homozygous	117019523
10	87260605	87260606	G	A	18	GENIC	possibly homozygous	117019524
10	87260705	87260706	A	C	16	GENIC	homozygous	117019525
10	87260727	87260728	C	T	19	GENIC	homozygous	117019526
10	87260775	87260776	G	A	15	GENIC	homozygous	117019527
10	87260860	87260861	A	G	19	GENIC	possibly homozygous	117019528
10	87260955	87260956	T	C	11	GENIC	homozygous	116817517
10	87261191	87261192	C	T	27	GENIC	possibly homozygous	117019529
10	87261508	87261509	A	G	21	GENIC	homozygous	117019530