chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	13692226	13692227	A	G	47	GENIC	homozygous	119770636
20	13692278	13692279	C	T	53	GENIC	homozygous	119770638
20	13692680	13692681	G	A	62	GENIC	homozygous	119770640
20	13692773	13692774	A	G	49	GENIC	homozygous	119770642
20	13692835	13692836	C	T	50	GENIC	homozygous	119770644
20	13692888	13692889	A	G	64	GENIC	heterozygous	119770645
20	13693107	13693108	T	C	82	GENIC	homozygous	119770647
20	13693174	13693175	G	T	52	GENIC	homozygous	119770649
20	13694408	13694409	T	G	50	GENIC	homozygous	119770651
20	13694651	13694652	A	G	59	GENIC	homozygous	119770653
20	13695444	13695445	A	T	62	GENIC	possibly homozygous	119770655
20	13695807	13695808	T	G	55	GENIC	homozygous	119770657
20	13696179	13696180	G	A	46	GENIC	homozygous	119770658
20	13696417	13696418	C	A	49	GENIC	possibly homozygous	119770660
20	13697845	13697846	A	G	55	GENIC	homozygous	119770662
20	13697914	13697915	A	G	69	GENIC	homozygous	119770664
20	13698416	13698417	G	A	67	GENIC	homozygous	119770666
20	13699570	13699571	T	C	52	GENIC	homozygous	119770668
20	13699785	13699786	G	C	50	GENIC	homozygous	119770670
20	13701104	13701105	C	T	58	GENIC	possibly homozygous	119770672
20	13701118	13701119	G	A	50	GENIC	possibly homozygous	119770674
20	13701434	13701435	C	T	43	GENIC	homozygous	119770676
20	13702719	13702720	G	A	44	GENIC	homozygous	119770678
20	13702933	13702934	T	C	55	GENIC	homozygous	119770680
20	13703291	13703292	T	C	61	GENIC	homozygous	119770682
20	13706073	13706074	T	C	42	GENIC	possibly homozygous	119770684
20	13706782	13706783	G	A	52	GENIC	homozygous	119770686
20	13706829	13706830	G	A	48	GENIC	possibly homozygous	119770688
20	13707599	13707600	C	A	55	GENIC	homozygous	119770690
20	13707639	13707640	T	A	51	GENIC	homozygous	119770692