chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	31892563	31892564	G	A	11	GENIC	homozygous	46051987
20	31892656	31892657	G	A	15	GENIC	homozygous	46051989
20	31893470	31893471	T	C	26	GENIC	homozygous	45521083
20	31893703	31893704	T	C	16	GENIC	homozygous	46051991
20	31894750	31894751	T	C	16	GENIC	homozygous	45740951
20	31895248	31895249	G	T	12	GENIC	homozygous	46051993
20	31895284	31895285	G	GT	8	GENIC	homozygous	46051995
20	31896042	31896043	C	G	16	GENIC	homozygous	45521087
20	31896321	31896322	A	AATC	14	GENIC	homozygous	45521089
20	31897519	31897520	G	GGACA	21	GENIC	homozygous	45521091
20	31898250	31898251	T	C	9	GENIC	homozygous	45521105
20	31898708	31898709	G	A	19	GENIC	homozygous	45740959
20	31898950	31898951	C	T	21	GENIC	homozygous	45740961
20	31898992	31898993	C	T	22	GENIC	homozygous	45740963
20	31901809	31901810	C	T	20	GENIC	homozygous	45740965
20	31901862	31901863	G	C	25	GENIC	homozygous	45521115
20	31902038	31902039	G	T	21	GENIC	homozygous	45740967
20	31902222	31902223	C	T	14	GENIC	homozygous	45740969
20	31903751	31903752	T	C	18	GENIC	homozygous	45521121
20	31905147	31905148	A	G	9	GENIC	homozygous	45740970