chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	124872673	124872674	G	A	29	GENIC	possibly homozygous	112147880
3	124874137	124874138	T	C	43	GENIC	homozygous	111694932
3	124874232	124874233	T	G	48	GENIC	homozygous	112147882
3	124874413	124874414	G	A	28	GENIC	homozygous	112147884
3	124874520	124874521	T	C	38	GENIC	homozygous	111694936
3	124874903	124874904	G	A	32	GENIC	homozygous	112147886
3	124874977	124874978	A	G	37	GENIC	homozygous	112147888
3	124875002	124875003	T	G	38	GENIC	homozygous	112147890
3	124875011	124875012	A	C	35	GENIC	homozygous	111694937
3	124875438	124875439	G	A	38	GENIC	homozygous	112147892
3	124875533	124875534	G	A	33	GENIC	homozygous	111694941
3	124875586	124875587	A	G	29	GENIC	homozygous	111694942
3	124877739	124877740	G	A	45	GENIC	possibly homozygous	112147894
3	124878477	124878478	T	C	43	GENIC	homozygous	111694946
3	124879247	124879248	C	T	28	GENIC	possibly homozygous	111694947