chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
10	55013851	55013852	G	A	11	GENIC	homozygous	116602024
10	55014707	55014708	G	C	29	GENIC	homozygous	116602029
10	55014770	55014771	G	A	21	GENIC	homozygous	116602031
10	55014914	55014915	C	A	12	GENIC	homozygous	116602033
10	55015086	55015087	C	T	35	GENIC	homozygous	116602035
10	55015464	55015465	G	A	25	GENIC	homozygous	116602039
10	55015624	55015625	A	T	15	GENIC	homozygous	116890174
10	55015893	55015894	C	T	15	GENIC	homozygous	116602041
10	55016397	55016398	A	G	16	GENIC	homozygous	116602045
10	55016633	55016634	A	G	20	GENIC	homozygous	116602047
10	55016651	55016652	C	G	18	GENIC	homozygous	116602049
10	55016669	55016670	G	T	17	GENIC	homozygous	116602051
10	55018809	55018810	G	A	21	GENIC	homozygous	116781601
10	55018914	55018915	T	C	21	GENIC	homozygous	116781603
10	55020872	55020873	A	G	18	GENIC	homozygous	116602057
10	55023802	55023803	G	T	21	GENIC	homozygous	116890176
10	55024110	55024111	T	G	18	GENIC	homozygous	116890178
10	55024720	55024721	G	A	20	GENIC	homozygous	116890180
10	55027236	55027237	T	A	35	GENIC	homozygous	116602067
10	55027896	55027897	C	G	17	GENIC	homozygous	116602069
10	55028532	55028533	C	T	27	GENIC	homozygous	116602071
10	55030158	55030159	G	A	20	GENIC	homozygous	116602073
10	55030286	55030287	C	G	9	GENIC	homozygous	116602075
10	55030665	55030666	A	G	15	GENIC	homozygous	116602077
10	55031923	55031924	G	T	25	GENIC	homozygous	116602079
10	55045149	55045150	G	T	2	GENIC	homozygous	116781695
10	55045151	55045152	C	T	2	GENIC	homozygous	116781697
10	55049154	55049155	G	A	17	GENIC	homozygous	116602083
10	55073121	55073122	C	T	16	GENIC	homozygous	116602087