chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	157683346	157683347	T	C	70	GENIC	homozygous	112906898
4	157685548	157685548		TCCGTCCGTCCGTCCATCCA	67	GENIC	homozygous	131364161
4	157690378	157690379	A	G	52	GENIC	homozygous	112906906
4	157690573	157690574	G	A	57	GENIC	homozygous	113400722
4	157687125	157687126	C	T	46	GENIC	possibly homozygous	113400714
4	157688718	157688719	C	T	71	GENIC	possibly homozygous	113400716
4	157689146	157689147	T	C	74	GENIC	homozygous	113400718
4	157690306	157690307	T	C	66	GENIC	homozygous	113400720
4	157688614	157688614		T	74	GENIC	homozygous	128096227
4	157692682	157692683	C	G	58	GENIC	homozygous	113400724
4	157693342	157693343	G	A	75	GENIC	homozygous	113400726
4	157693884	157693885	C	T	57	GENIC	homozygous	113400728
4	157695076	157695077	C	T	49	GENIC	homozygous	113400730
4	157698151	157698152	G	A	53	GENIC	homozygous	113400732
4	157701545	157701546	C	T	59	GENIC	homozygous	113400734
4	157705347	157705348	A	G	51	GENIC	homozygous	113184586