chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
5	156998341	156998342	T	C	11	GENIC	homozygous	71175626
5	156999712	156999713	T	C	36	GENIC	possibly homozygous	71175628
5	157001539	157001540	A	T	33	GENIC	homozygous	71175630
5	157002347	157002348	T	C	14	GENIC	homozygous	71175632
5	157002855	157002856	T	C	29	GENIC	homozygous	71175634
5	157003741	157003742	T	C	28	GENIC	homozygous	71175636
5	157007249	157007250	C	T	14	GENIC	homozygous	71175638
5	157008772	157008773	T	C	21	GENIC	homozygous	71175642
5	157008773	157008774	T	C	20	GENIC	homozygous	71175644
5	157011489	157011490	A	G	19	GENIC	homozygous	71175646
5	157012069	157012070	T	C	17	GENIC	homozygous	71175648
5	157012352	157012353	G	A	33	GENIC	homozygous	71175650
5	157016998	157016999	G	A	25	GENIC	homozygous	71175658
5	157017454	157017455	A	G	27	GENIC	homozygous	71175660
5	157017505	157017506	C	T	33	GENIC	homozygous	72692206
5	157017506	157017507	T	A	33	GENIC	homozygous	71175662
5	157019029	157019030	C	T	30	GENIC	homozygous	71470391
5	157019113	157019114	A	G	19	GENIC	homozygous	71175676
5	157021592	157021593	G	A	19	GENIC	homozygous	71175678
5	157021880	157021881	C	G	25	GENIC	possibly homozygous	71175680
5	157022539	157022540	C	T	27	GENIC	homozygous	71175682
5	157022575	157022576	T	C	16	GENIC	homozygous	71175684
5	157022617	157022618	C	T	15	GENIC	homozygous	71175686
5	157023064	157023065	A	G	33	GENIC	homozygous	71175688
5	157023295	157023296	A	G	31	GENIC	possibly homozygous	71175690