chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	262038442	262038443	C	T	16	GENIC	possibly homozygous	61638764
1	262039436	262039437	A	C	9	GENIC	possibly homozygous	61182468
1	262039533	262039534	T	C	9	GENIC	possibly homozygous	61638765
1	262040405	262040406	C	T	11	GENIC	possibly homozygous	61182470
1	262040531	262040532	T	G	16	GENIC	homozygous	61182471
1	262041205	262041206	C	T	12	GENIC	possibly homozygous	61638767
1	262041696	262041697	G	C	18	GENIC	homozygous	61182472
1	262042103	262042104	C	A	10	GENIC	homozygous	61182476
1	262042735	262042736	A	G	15	GENIC	homozygous	61182477
1	262043051	262043052	C	T	28	GENIC	homozygous	61638768
1	262043375	262043376	A	G	14	GENIC	homozygous	61182478
1	262043456	262043457	G	T	12	GENIC	homozygous	61182479
1	262043752	262043753	C	CT	6	GENIC	heterozygous	61638769
1	262043769	262043770	A	T	4	GENIC	heterozygous	61638770
1	262043770	262043771	A	T	4	GENIC	heterozygous	61638771
1	262043850	262043851	G	A	2	GENIC	homozygous	61182481
1	262044092	262044095	CCT	---	2	GENIC	homozygous	61182486
1	262044197	262044198	G	T	16	GENIC	homozygous	61182487
1	262045620	262045622	TT	--	2	GENIC	heterozygous	61182495
1	262045654	262045655	G	T	16	GENIC	homozygous	61638778
1	262045782	262045783	C	T	12	GENIC	heterozygous	61638779
1	262046560	262046561	G	A	13	GENIC	possibly homozygous	61638780
1	262046655	262046656	C	T	12	GENIC	homozygous	61638781