chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	105306250	105306251	C	G	8	GENIC	homozygous	118012473
10	105306368	105306369	A	C	10	GENIC	homozygous	116836510
10	105306424	105306425	G	T	19	GENIC	homozygous	116908676
10	105306502	105306503	A	G	16	GENIC	possibly homozygous	118012474
10	105308679	105308680	G	T	38	GENIC	homozygous	116713820
10	105309366	105309367	A	G	8	GENIC	homozygous	118012475
10	105309811	105309812	T	G	28	GENIC	homozygous	117414542
10	105309813	105309814	T	G	28	GENIC	homozygous	117414544
10	105309937	105309938	C	T	27	GENIC	homozygous	117031677
10	105310010	105310011	A	C	17	GENIC	homozygous	117031679
10	105310165	105310166	C	G	15	GENIC	homozygous	118012478
10	105329364	105329365	A	G	8	GENIC	homozygous	117089115
10	105335254	105335255	T	G	15	GENIC	homozygous	118012481
10	105335294	105335295	T	G	5	GENIC	homozygous	118012482
10	105358260	105358261	A	G	4	GENIC	homozygous	116836603
10	105358400	105358401	A	C	9	GENIC	homozygous	117089117
10	105358822	105358823	A	C	4	GENIC	homozygous	116713834
10	105358847	105358848	A	C	4	GENIC	homozygous	118012484
10	105363546	105363547	T	C	18	GENIC	heterozygous	118012485
10	105365369	105365370	A	G	13	GENIC	heterozygous	118012486
10	105365384	105365385	C	T	12	GENIC	heterozygous	118012487
10	105309965	105309966	C	A	18	GENIC	homozygous	116961688