chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	117183108	117183109	T	C	8	GENIC	homozygous	116671090
8	117183890	117183891	T	C	10	GENIC	homozygous	116671092
8	117184246	117184247	G	A	5	GENIC	homozygous	117920277
8	117184377	117184378	C	T	10	GENIC	homozygous	117920278
8	117184516	117184517	G	C	8	GENIC	homozygous	116671094
8	117185658	117185659	A	G	9	GENIC	homozygous	117920279
8	117186602	117186603	T	C	11	GENIC	homozygous	116671098
8	117187259	117187260	T	C	13	GENIC	homozygous	116671100
8	117187317	117187318	G	C	9	GENIC	homozygous	117920280
8	117187620	117187621	T	C	12	GENIC	homozygous	116671102
8	117189683	117189684	C	T	10	GENIC	homozygous	117920281
8	117189794	117189795	G	A	6	GENIC	homozygous	117920282
8	117190737	117190738	C	T	10	GENIC	homozygous	117920283
8	117190861	117190862	A	G	17	GENIC	homozygous	116671110
8	117193586	117193587	T	G	5	GENIC	homozygous	117920284
8	117193803	117193804	G	T	9	GENIC	homozygous	116671114
8	117201088	117201089	G	A	14	GENIC	homozygous	117920285
8	117209604	117209605	G	A	7	GENIC	homozygous	117920286
8	117209742	117209743	A	G	6	GENIC	homozygous	116671130
8	117209919	117209920	C	T	8	GENIC	homozygous	116671136
8	117210100	117210101	C	G	5	GENIC	homozygous	116671138
8	117212612	117212613	G	A	13	GENIC	homozygous	116671148
8	117212839	117212840	A	G	11	GENIC	homozygous	116671150
8	117213124	117213125	G	A	17	GENIC	possibly homozygous	117920287
8	117213423	117213424	C	T	14	GENIC	homozygous	117920288
8	117214922	117214923	G	A	3	GENIC	homozygous	117920289