chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	145118741	145118742	A	G	21	GENIC	homozygous	126101650
4	145119403	145119404	T	A	11	GENIC	homozygous	112870628
4	145119523	145119524	G	C	23	GENIC	homozygous	112870629
4	145119728	145119729	T	A	21	GENIC	homozygous	126101652
4	145119998	145119999	T	C	18	GENIC	homozygous	112870630
4	145121377	145121378	G	A	12	GENIC	homozygous	112870633
4	145123158	145123159	T	C	21	GENIC	homozygous	112870634
4	145123623	145123624	G	T	19	GENIC	homozygous	112870635
4	145124114	145124115	A	G	9	GENIC	homozygous	112870636
4	145125968	145125969	C	T	13	GENIC	homozygous	112870637
4	145126827	145126828	C	T	11	GENIC	homozygous	112870638
4	145128123	145128124	G	A	14	GENIC	homozygous	126101654
4	145128813	145128814	C	A	14	GENIC	homozygous	126101656
4	145128992	145128993	G	A	10	GENIC	homozygous	126101658
4	145129031	145129032	G	A	11	GENIC	homozygous	126024897
4	145129405	145129406	A	G	13	GENIC	homozygous	126101660
4	145129833	145129834	T	C	20	GENIC	homozygous	126024901
4	145133239	145133240	A	G	17	GENIC	homozygous	126101662
4	145134049	145134050	C	T	8	GENIC	homozygous	126101664
4	145134090	145134091	A	G	15	GENIC	homozygous	126024902
4	145134350	145134351	C	T	14	GENIC	homozygous	126024903
4	145134873	145134874	G	A	26	GENIC	homozygous	126101666
4	145143668	145143669	C	T	25	GENIC	homozygous	126101667
4	145146498	145146499	A	G	4	GENIC	homozygous	112870642