chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
3	156731150	156731151	G	C	71	GENIC	homozygous	112190691
3	156734081	156734082	T	C	51	GENIC	homozygous	112190692
3	156735132	156735133	A	G	41	GENIC	possibly homozygous	112190693
3	156737496	156737497	G	C	49	GENIC	homozygous	112190695
3	156738922	156738922		A	34	GENIC	possibly homozygous	132590018
3	156740877	156740878	G	C	44	GENIC	possibly homozygous	112190696
3	156740946	156740946		GCGTGTGCGTGTGCGTGTGCGTGTGC	22	GENIC	possibly homozygous	132590019
3	156743572	156743573	C	G	52	GENIC	homozygous	112190698
3	156743947	156743948	G	T	53	GENIC	homozygous	112190699
3	156744314	156744315	A		54	GENIC	homozygous	132590020
3	156744390	156744391	C	A	63	GENIC	homozygous	112190700
3	156744540	156744541	T	C	33	GENIC	homozygous	112190701
3	156744580	156744580		GCTGAG	37	GENIC	homozygous	132590021
3	156745378	156745379	G	A	38	GENIC	homozygous	112190702
3	156745730	156745730		CG	4	GENIC	homozygous	132590022
3	156747113	156747114	C	T	48	GENIC	homozygous	112190703
3	156747163	156747164	G	A	45	GENIC	homozygous	112190704
3	156747560	156747561	G	A	40	GENIC	homozygous	112190705
3	156748629	156748630	T	C	48	GENIC	homozygous	112190706
3	156749287	156749287		T	11	GENIC	homozygous	132590023
3	156750307	156750308	G	A	48	GENIC	homozygous	112190707
3	156750414	156750415	A	G	45	GENIC	homozygous	112190708
3	156751190	156751191	C	A	52	GENIC	homozygous	112190709
3	156752455	156752456	G	A	45	GENIC	homozygous	112190710
3	156752847	156752848	C	T	52	GENIC	homozygous	112190711
3	156753028	156753029	G	A	52	GENIC	homozygous	112190712
3	156754109	156754109		G	62	GENIC	homozygous	132590024
3	156755616	156755617	G	A	50	GENIC	homozygous	112190713
3	156756547	156756548	G	T	44	GENIC	homozygous	112190714
3	156757799	156757799		TT	36	GENIC	homozygous	132590025