chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	55013851	55013852	G	A	42	GENIC	homozygous	116602024
10	55014097	55014098	G	A	28	GENIC	homozygous	117195965
10	55014330	55014331	A	G	39	GENIC	homozygous	116602025
10	55014339	55014340	C	T	39	GENIC	homozygous	116602027
10	55014707	55014708	G	C	24	GENIC	homozygous	116602029
10	55014770	55014771	G	A	25	GENIC	possibly homozygous	116602031
10	55014914	55014915	C	A	35	GENIC	homozygous	116602033
10	55015086	55015087	C	T	24	GENIC	homozygous	116602035
10	55015111	55015112	C	T	25	GENIC	homozygous	116602037
10	55015464	55015465	G	A	28	GENIC	homozygous	116602039
10	55015893	55015894	C	T	19	GENIC	homozygous	116602041
10	55015983	55015984	G	A	10	GENIC	homozygous	116602043
10	55016397	55016398	A	G	17	GENIC	homozygous	116602045
10	55016633	55016634	A	G	23	GENIC	homozygous	116602047
10	55016651	55016652	C	G	25	GENIC	homozygous	116602049
10	55016669	55016670	G	T	24	GENIC	homozygous	116602051
10	55018517	55018518	T	C	31	GENIC	homozygous	116602053
10	55019076	55019077	T	A	29	GENIC	homozygous	116602055
10	55020872	55020873	A	G	13	GENIC	homozygous	116602057
10	55022482	55022483	G	A	29	GENIC	homozygous	116602059
10	55024443	55024444	G	A	22	GENIC	homozygous	117195968
10	55025553	55025554	G	T	32	GENIC	homozygous	116602061
10	55025811	55025812	T	A	27	GENIC	homozygous	116602063
10	55025836	55025837	T	A	20	GENIC	homozygous	116602065
10	55027236	55027237	T	A	13	GENIC	homozygous	116602067
10	55028532	55028533	C	T	20	GENIC	homozygous	116602071
10	55030158	55030159	G	A	22	GENIC	homozygous	116602073
10	55030286	55030287	C	G	30	GENIC	homozygous	116602075
10	55030665	55030666	A	G	19	GENIC	homozygous	116602077
10	55031923	55031924	G	T	10	GENIC	homozygous	116602079
10	55033533	55033534	G	C	23	GENIC	homozygous	116781649
10	55049154	55049155	G	A	23	GENIC	homozygous	116602083
10	55073121	55073122	C	T	35	GENIC	homozygous	116602087
10	55029719	55029720	C	T	2	GENIC	homozygous	117218739