chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
7	12410046	12410047	T	C	43	GENIC	possibly homozygous	53790877
7	12410421	12410422	C	T	29	GENIC	homozygous	54630294
7	12411043	12411044	G	A	35	GENIC	heterozygous	53790879
7	12411060	12411061	T	C	32	GENIC	possibly homozygous	53790881
7	12411115	12411116	T	TGAG	13	GENIC	heterozygous	53790886
7	12411150	12411151	T	A	13	GENIC	heterozygous	54181774
7	12411506	12411507	T	C	25	GENIC	possibly homozygous	53790887
7	12411707	12411708	G	A	23	GENIC	homozygous	53790888
7	12411708	12411709	T	G	23	GENIC	homozygous	54630296
7	12412179	12412180	T	C	57	GENIC	homozygous	53790889
7	12412390	12412391	A	AG	12	GENIC	homozygous	54630298
7	12413026	12413027	C	T	29	GENIC	homozygous	53790892
7	12414009	12414010	A	T	43	GENIC	homozygous	53790894
7	12414359	12414362	GGG	---	26	GENIC	homozygous	53790895
7	12415928	12415929	C	T	52	GENIC	homozygous	54630300
7	12415948	12415949	G	T	52	GENIC	homozygous	54630302
7	12416346	12416347	G	T	34	GENIC	homozygous	53790897
7	12416359	12416360	C	A	33	GENIC	homozygous	53790898