chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	31892711	31892712	G	A	16	GENIC	homozygous	45521081
20	31893470	31893471	T	C	25	GENIC	homozygous	45521083
20	31893587	31893588	G	A	12	GENIC	possibly homozygous	45521085
20	31896042	31896043	C	G	25	GENIC	homozygous	45521087
20	31896321	31896322	A	AATC	14	GENIC	heterozygous	45521089
20	31897519	31897520	G	GGACA	6	GENIC	heterozygous	45521091
20	31898029	31898030	C	A	1	GENIC	homozygous	45521103
20	31898250	31898251	T	C	17	GENIC	possibly homozygous	45521105
20	31898383	31898384	A	G	22	GENIC	homozygous	45521107
20	31898530	31898531	A	C	17	GENIC	homozygous	45521109
20	31899905	31899906	G	A	22	GENIC	possibly homozygous	45521111
20	31901688	31901689	A	AT	2	GENIC	homozygous	45521113
20	31901862	31901863	G	C	22	GENIC	homozygous	45521115
20	31902908	31902909	T	TG	8	GENIC	heterozygous	45521117
20	31903580	31903581	C	T	21	GENIC	possibly homozygous	45521119
20	31903751	31903752	T	C	23	GENIC	homozygous	45521121
20	31905033	31905049	GTGTGTGTGTGTGTGT	----------------	3	GENIC	homozygous	45898536