chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	145413431	145413432	C	A	26	GENIC	possibly homozygous	119412393
4	145414313	145414314	G	T	27	GENIC	possibly homozygous	119412394
4	145414901	145414902	C	A	43	GENIC	homozygous	112870864
4	145416140	145416141	C	T	10	GENIC	homozygous	119315486
4	145417452	145417453	C	T	14	GENIC	possibly homozygous	119315488
4	145418325	145418326	A	G	38	GENIC	possibly homozygous	119315489
4	145418407	145418408	A	G	35	GENIC	possibly homozygous	119412395
4	145418851	145418852	C	T	29	GENIC	homozygous	119315490
4	145419175	145419176	C	T	36	GENIC	homozygous	119315491
4	145419283	145419284	T	G	30	GENIC	possibly homozygous	119315492
4	145419403	145419404	C	T	27	GENIC	possibly homozygous	119315493
4	145419565	145419566	T	C	27	GENIC	homozygous	119315494
4	145420010	145420011	T	C	25	GENIC	possibly homozygous	119315495
4	145420150	145420151	C	T	26	GENIC	possibly homozygous	119315501
4	145420174	145420175	C	G	20	GENIC	possibly homozygous	119315502
4	145420219	145420220	C	T	25	GENIC	homozygous	119315503
4	145420220	145420221	C	G	24	GENIC	homozygous	119315504
4	145420383	145420384	A	G	27	GENIC	homozygous	119315505
4	145420750	145420751	T	C	12	GENIC	homozygous	119315506
4	145420787	145420788	T	C	18	GENIC	homozygous	119412396
4	145420992	145420993	A	C	17	GENIC	homozygous	119315507
4	145421024	145421025	C	T	15	GENIC	homozygous	119315508
4	145422080	145422081	C	G	32	GENIC	possibly homozygous	119587736
4	145423225	145423226	A	G	24	GENIC	homozygous	112870866
4	145424668	145424669	A	G	18	GENIC	homozygous	112870868
4	145424883	145424884	T	A	26	GENIC	homozygous	112870869
4	145425443	145425444	A	G	15	GENIC	homozygous	112870871
4	145425830	145425831	T	G	20	GENIC	homozygous	113178978