chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
2	237589127	237589128	G	T	12	GENIC	homozygous	60522205
2	237589190	237589191	G	A	12	GENIC	homozygous	59946719
2	237590150	237590151	A	G	21	GENIC	homozygous	59455701
2	237590500	237590501	C	A	20	GENIC	homozygous	59946720
2	237590572	237590573	C	G	26	GENIC	possibly homozygous	59946721
2	237590573	237590574	T	A	26	GENIC	possibly homozygous	59946722
2	237590590	237590593	AAA	---	8	GENIC	heterozygous	59776855
2	237590591	237590593	AA	--	8	GENIC	heterozygous	60522206
2	237590841	237590842	T	C	16	GENIC	homozygous	59455705
2	237592323	237592324	C	T	24	GENIC	homozygous	59946723
2	237592890	237592891	G	A	22	GENIC	homozygous	59946724
2	237593349	237593350	C	T	28	GENIC	homozygous	59946725
2	237594164	237594165	A	G	9	GENIC	homozygous	59455709
2	237594995	237594996	G	A	24	GENIC	homozygous	59946726
2	237595322	237595323	C	CT	2	GENIC	homozygous	60522207
2	237596164	237596165	A	T	28	GENIC	possibly homozygous	59455711
2	237596273	237596274	T	C	18	GENIC	homozygous	59455712
2	237597645	237597646	C	T	26	GENIC	homozygous	59946727
2	237598144	237598145	A	G	25	GENIC	homozygous	59946728
2	237600459	237600460	T	G	27	GENIC	homozygous	59946729
2	237600684	237600685	T	C	23	GENIC	homozygous	59946730