chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	252487521	252487522	T	C	18	GENIC	homozygous	108612105
1	252488647	252488648	C	T	42	GENIC	homozygous	108612106
1	252489014	252489015	G	A	36	GENIC	homozygous	108612107
1	252489800	252489801	G	A	38	GENIC	homozygous	108612108
1	252491088	252491089	C	G	35	GENIC	homozygous	108612109
1	252492011	252492012	T	A	32	GENIC	homozygous	108612110
1	252493939	252493940	G	T	29	GENIC	homozygous	108612111
1	252494608	252494609	T	C	30	GENIC	homozygous	108612112
1	252494684	252494685	C	T	31	GENIC	homozygous	108612113
1	252494864	252494865	A	G	26	GENIC	homozygous	108612114
1	252495331	252495332	C	T	36	GENIC	homozygous	108612115
1	252495336	252495337	G	A	40	GENIC	homozygous	108612116
1	252495342	252495343	C	T	43	GENIC	homozygous	108612117
1	252495898	252495899	T	A	43	GENIC	homozygous	108612118
1	252495905	252495906	A	T	41	GENIC	homozygous	108612119
1	252496281	252496282	C	T	37	GENIC	homozygous	108612120
1	252496792	252496793	T	A	55	GENIC	homozygous	108612121
1	252497134	252497135	G	A	39	GENIC	homozygous	108612122
1	252497253	252497254	A	T	39	GENIC	homozygous	108612123
1	252497257	252497258	T	C	40	GENIC	homozygous	108612124
1	252497258	252497259	C	T	41	GENIC	homozygous	108612125