chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	220863861	220863862	G	T	6	GENIC	homozygous	57099136
4	220865950	220865951	T	C	26	GENIC	possibly homozygous	57099138
4	220866308	220866309	C	T	13	GENIC	possibly homozygous	57099140
4	220867182	220867183	C	T	27	GENIC	homozygous	57099141
4	220867457	220867458	G	T	22	GENIC	possibly homozygous	57099142
4	220867545	220867546	A	T	7	GENIC	homozygous	57099143
4	220870021	220870022	T	C	24	GENIC	homozygous	57099145
4	220870972	220870973	A	ATTTT	1	GENIC	homozygous	57099146
4	220873146	220873147	T	C	21	GENIC	homozygous	57099152
4	220873953	220873954	T	C	19	GENIC	homozygous	57099154
4	220875728	220875729	T	TA	7	GENIC	possibly homozygous	57099158
4	220877136	220877137	G	GTCTCTC	1	GENIC	homozygous	57099160
4	220877271	220877272	C	G	4	GENIC	homozygous	57099165
4	220879291	220879292	G	A	12	GENIC	possibly homozygous	57099175
4	220880183	220880184	C	T	18	GENIC	possibly homozygous	57099176
4	220880485	220880486	G	A	29	GENIC	homozygous	57099177
4	220880567	220880568	A	G	10	GENIC	homozygous	57099178
4	220880591	220880592	A	C	11	GENIC	homozygous	57099179