chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
4	85187551	85187552	G	A	26	GENIC	homozygous	113279025
4	85187631	85187632	T	C	16	GENIC	homozygous	113279027
4	85188989	85188990	A	G	29	GENIC	homozygous	113279028
4	85189030	85189031	A	G	23	GENIC	homozygous	113279030
4	85189605	85189606	C	T	30	GENIC	homozygous	113279032
4	85190079	85190080	G	A	43	GENIC	homozygous	113279034
4	85190084	85190085	G	A	46	GENIC	homozygous	113279036
4	85190723	85190724	T	C	26	GENIC	homozygous	113279038
4	85190788	85190789	C	T	19	GENIC	homozygous	113279040
4	85191123	85191124	T	A	33	GENIC	homozygous	113279041
4	85191269	85191270	C	A	45	GENIC	homozygous	113279043
4	85191538	85191539	A	G	25	GENIC	homozygous	113279045
4	85191628	85191629	A	G	36	GENIC	possibly homozygous	113279047
4	85192196	85192197	C	T	41	GENIC	homozygous	113279049
4	85192296	85192297	T	A	35	GENIC	homozygous	113279051
4	85192745	85192746	G	A	16	GENIC	homozygous	113279053