chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
8	82288767	82288768	T	C	12	GENIC	homozygous	116531644
8	82289185	82289186	A	G	25	GENIC	homozygous	116531646
8	82289235	82289236	C	T	20	GENIC	homozygous	116531648
8	82289246	82289247	G	A	22	GENIC	homozygous	116531650
8	82289291	82289292	C	T	28	GENIC	homozygous	116531652
8	82289638	82289639	T	C	18	GENIC	homozygous	116531656
8	82289682	82289683	A	G	15	GENIC	homozygous	116531658
8	82289701	82289702	A	C	15	GENIC	homozygous	116531660
8	82289832	82289833	G	A	21	GENIC	homozygous	116531662
8	82291033	82291034	A	G	24	GENIC	possibly homozygous	116531666
8	82291119	82291120	C	A	31	GENIC	homozygous	116531668
8	82293675	82293676	T	C	28	GENIC	homozygous	116531676
8	82294280	82294281	C	G	18	GENIC	homozygous	116531678
8	82294457	82294458	T	C	17	GENIC	homozygous	116531680
8	82294478	82294479	T	C	20	GENIC	homozygous	116531682
8	82294668	82294669	C	T	13	GENIC	homozygous	116531684