chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
1	57492288	57492289	T	C	28	GENIC	homozygous	108111642
1	57492779	57492780	T	G	24	GENIC	homozygous	108111643
1	57495629	57495630	A	G	18	GENIC	homozygous	108111644
1	57498406	57498407	T	G	17	GENIC	homozygous	108111646
1	57499743	57499744	G	A	20	GENIC	homozygous	108111649
1	57500368	57500369	A	G	27	GENIC	homozygous	108111652
1	57500468	57500469	A	G	22	GENIC	homozygous	108111653
1	57500942	57500943	T	C	24	GENIC	homozygous	108111654
1	57501061	57501062	C	T	29	GENIC	homozygous	108111655
1	57501829	57501830	T	C	30	GENIC	homozygous	108111656
1	57502296	57502297	A	G	30	GENIC	homozygous	108111657
1	57503250	57503251	G	A	24	GENIC	homozygous	108111658
1	57505844	57505845	C	T	44	GENIC	homozygous	108111659
1	57506900	57506901	G	A	27	GENIC	homozygous	108111660
1	57506934	57506935	G	A	30	GENIC	homozygous	108111661
1	57507198	57507199	G	A	20	GENIC	homozygous	108111662
1	57507292	57507293	A	C	29	GENIC	homozygous	108857455
1	57507953	57507954	A	G	22	GENIC	homozygous	108111663
1	57508557	57508558	C	T	35	GENIC	homozygous	108111664
1	57508904	57508905	G	A	32	GENIC	homozygous	108111665
1	57509291	57509292	G	A	42	GENIC	homozygous	108111666