chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	148469893	148469894	C	A	30	GENIC	possibly homozygous	112876014
4	148469954	148469955	C	T	27	GENIC	homozygous	112876016
4	148470374	148470375	A	G	20	GENIC	homozygous	112876018
4	148470666	148470667	T	C	12	GENIC	homozygous	112876019
4	148471188	148471189	T	C	16	GENIC	homozygous	112876021
4	148471826	148471827	A	G	19	GENIC	homozygous	112876023
4	148471905	148471906	G	T	19	GENIC	homozygous	113562862
4	148471906	148471907	A	G	19	GENIC	homozygous	119281804
4	148472123	148472124	C	T	34	GENIC	homozygous	112876024
4	148472130	148472131	C	T	30	GENIC	homozygous	112876026
4	148472208	148472209	G	A	23	GENIC	homozygous	112876028
4	148473488	148473489	A	G	20	GENIC	homozygous	112876031
4	148473533	148473534	T	C	16	GENIC	homozygous	112876032
4	148473661	148473662	A	C	24	GENIC	homozygous	112876034
4	148473790	148473791	A	G	22	GENIC	possibly homozygous	112876036
4	148474070	148474071	A	G	39	GENIC	homozygous	112876037
4	148474075	148474076	C	T	37	GENIC	homozygous	112876039
4	148474287	148474288	A	G	37	GENIC	homozygous	112876044
4	148474141	148474142	T	C	39	GENIC	homozygous	112876041
4	148474205	148474206	T	A	34	GENIC	homozygous	112876042
4	148474449	148474450	C	T	35	GENIC	homozygous	112876045
4	148474614	148474615	C	T	20	GENIC	homozygous	112876047
4	148474665	148474666	G	A	30	GENIC	homozygous	112876048
4	148474873	148474874	T	G	33	GENIC	homozygous	112876050
4	148475115	148475116	T	C	38	GENIC	homozygous	112876052
4	148475292	148475293	A	T	30	GENIC	homozygous	112876053
4	148477173	148477174	A	C	28	GENIC	homozygous	112876055