chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	157821884	157821885	T	C	44	GENIC	homozygous	114070486
5	157822249	157822250	T	C	39	GENIC	homozygous	114070487
5	157823493	157823494	A	T	40	GENIC	possibly homozygous	114070488
5	157824249	157824250	A	T	41	GENIC	homozygous	114070489
5	157824331	157824332	G	A	55	GENIC	homozygous	114070490
5	157826521	157826522	A	G	35	GENIC	homozygous	114070491
5	157826918	157826919	A	C	42	GENIC	homozygous	114070492
5	157828070	157828071	G	A	46	GENIC	homozygous	114070493
5	157828072	157828073	C	A	46	GENIC	homozygous	114070494
5	157828794	157828795	A	G	46	GENIC	homozygous	114070495
5	157828896	157828897	T	G	50	GENIC	homozygous	114070496
5	157829333	157829334	T	C	35	GENIC	homozygous	114070497
5	157829684	157829685	G	A	44	GENIC	possibly homozygous	114070498
5	157829846	157829847	G	A	55	GENIC	homozygous	114070499
5	157830714	157830715	G	A	66	GENIC	homozygous	114070500
5	157831975	157831976	C	T	52	GENIC	homozygous	114070501
5	157837398	157837399	C	T	31	GENIC	homozygous	114070502
5	157837449	157837450	G	T	34	GENIC	homozygous	114070503
5	157837604	157837605	G	A	50	GENIC	homozygous	114070504
5	157837744	157837745	G	A	18	GENIC	homozygous	114070505
5	157838325	157838326	G	A	42	GENIC	homozygous	114070506
5	157839657	157839658	T	C	76	GENIC	homozygous	114070507
5	157841222	157841223	C	A	39	GENIC	homozygous	114070508
5	157842985	157842986	A	G	48	GENIC	homozygous	114070509
5	157846079	157846080	T	C	28	GENIC	heterozygous	114070510