chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	31892711	31892712	G	A	52	GENIC	homozygous	45521081
20	31893470	31893471	T	C	49	GENIC	possibly homozygous	45521083
20	31893587	31893588	G	A	61	GENIC	homozygous	45521085
20	31896042	31896043	C	G	63	GENIC	homozygous	45521087
20	31896321	31896322	A	AATC	60	GENIC	homozygous	45521089
20	31897519	31897520	G	GGACA	50	GENIC	homozygous	45521091
20	31897984	31897985	A	G	22	GENIC	heterozygous	45521093
20	31897996	31897999	AAC	---	21	GENIC	homozygous	45521095
20	31897998	31897999	C	-	22	GENIC	homozygous	45521097
20	31898008	31898009	C	-	24	GENIC	heterozygous	45521099
20	31898019	31898020	C	CAA	20	GENIC	homozygous	45521101
20	31898250	31898251	T	C	61	GENIC	homozygous	45521105
20	31898383	31898384	A	G	51	GENIC	homozygous	45521107
20	31898530	31898531	A	C	54	GENIC	possibly homozygous	45521109
20	31899905	31899906	G	A	60	GENIC	possibly homozygous	45521111
20	31901688	31901689	A	AT	53	GENIC	possibly homozygous	45521113
20	31901862	31901863	G	C	47	GENIC	homozygous	45521115
20	31902908	31902909	T	TG	23	GENIC	heterozygous	45521117
20	31903580	31903581	C	T	58	GENIC	homozygous	45521119
20	31903751	31903752	T	C	79	GENIC	homozygous	45521121