chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	61166298	61166299	G	C	29	GENIC	homozygous	116179131
7	61166351	61166352	T	G	28	GENIC	homozygous	116179133
7	61166902	61166903	T	C	27	GENIC	homozygous	116179135
7	61168429	61168430	T	C	22	GENIC	homozygous	116179137
7	61169135	61169136	T	C	14	GENIC	homozygous	116179139
7	61170317	61170318	T	G	18	GENIC	homozygous	116179141
7	61170379	61170380	A	T	25	GENIC	homozygous	116179143
7	61171075	61171076	G	A	25	GENIC	homozygous	116179145
7	61171532	61171533	T	C	17	GENIC	homozygous	116179147
7	61172081	61172082	C	T	38	GENIC	homozygous	116179149
7	61172625	61172626	T	A	32	GENIC	homozygous	116179151
7	61173266	61173267	G	A	19	GENIC	homozygous	116179153
7	61186418	61186419	C	T	28	GENIC	homozygous	116179155
7	61187610	61187611	C	T	26	GENIC	homozygous	116179157
7	61193478	61193479	G	A	11	GENIC	heterozygous	116179159
7	61193558	61193559	G	A	25	GENIC	heterozygous	116179161
7	61194178	61194179	A	G	20	GENIC	homozygous	115688777
7	61194313	61194314	A	G	10	GENIC	homozygous	115688778
7	61194377	61194378	T	G	20	GENIC	homozygous	115688779
7	61197978	61197979	T	C	25	GENIC	homozygous	116179163
7	61198433	61198434	C	G	16	GENIC	homozygous	116179165
7	61198601	61198602	T	A	22	GENIC	homozygous	116179167
7	61198696	61198697	G	A	27	GENIC	homozygous	116179169