chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	149261124	149261125	A	G	21	GENIC	homozygous	57516786
4	149261125	149261126	G	A	21	GENIC	homozygous	58285641
4	149261548	149261549	T	C	8	GENIC	homozygous	56977807
4	149262047	149262048	C	T	20	GENIC	homozygous	58086890
4	149262850	149262851	C	CTTCTCACAG	34	GENIC	homozygous	56977810
4	149262868	149262869	G	C	30	GENIC	homozygous	56977811
4	149263165	149263168	TGT	---	26	GENIC	homozygous	58086892
4	149263197	149263198	G	GGT	30	GENIC	possibly homozygous	57838730
4	149264038	149264039	C	T	22	GENIC	homozygous	58086894
4	149264090	149264091	G	A	12	GENIC	homozygous	56977816
4	149264147	149264149	CA	--	14	GENIC	homozygous	58345745
4	149264300	149264306	ATGTTT	------	21	GENIC	homozygous	56977817
4	149264306	149264307	A	C	21	GENIC	homozygous	58345747
4	149264309	149264310	A	AG	20	GENIC	homozygous	56977818
4	149264343	149264344	A	T	24	GENIC	homozygous	56977819
4	149264640	149264641	A	G	23	GENIC	homozygous	56977820
4	149264719	149264720	A	T	20	GENIC	possibly homozygous	58086897
4	149264856	149264857	T	C	29	GENIC	homozygous	56977822
4	149265082	149265083	C	A	23	GENIC	homozygous	58086899
4	149266377	149266378	A	T	23	GENIC	possibly homozygous	56977829
4	149267783	149267785	TG	--	15	GENIC	heterozygous	58528087