chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	31893470	31893471	T	C	19	GENIC	homozygous	45521083
20	31894064	31894065	T	C	24	GENIC	possibly homozygous	45740948
20	31894653	31894654	C	T	10	GENIC	homozygous	45740949
20	31894750	31894751	T	C	10	GENIC	homozygous	45740951
20	31895283	31895284	T	TG	2	GENIC	homozygous	45740953
20	31895296	31895297	T	TTC	3	GENIC	homozygous	45740955
20	31895540	31895541	A	G	21	GENIC	possibly homozygous	45740957
20	31896042	31896043	C	G	21	GENIC	homozygous	45521087
20	31896321	31896322	A	AATC	6	GENIC	homozygous	45521089
20	31897519	31897520	G	GGACA	9	GENIC	possibly homozygous	45521091
20	31898029	31898030	C	A	3	GENIC	heterozygous	45521103
20	31898250	31898251	T	C	20	GENIC	possibly homozygous	45521105
20	31898708	31898709	G	A	18	GENIC	homozygous	45740959
20	31898950	31898951	C	T	18	GENIC	possibly homozygous	45740961
20	31898992	31898993	C	T	14	GENIC	homozygous	45740963
20	31901809	31901810	C	T	13	GENIC	heterozygous	45740965
20	31901862	31901863	G	C	22	GENIC	possibly homozygous	45521115
20	31902038	31902039	G	T	19	GENIC	possibly homozygous	45740967
20	31902222	31902223	C	T	15	GENIC	homozygous	45740969
20	31903751	31903752	T	C	29	GENIC	homozygous	45521121
20	31905147	31905148	A	G	20	GENIC	possibly homozygous	45740970