chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	42967210	42967211	G	C	34	GENIC	homozygous	109202860
20	42967388	42967389	A	G	55	GENIC	homozygous	109202862
20	42968216	42968217	C	G	35	GENIC	homozygous	109270022
20	42968223	42968224	T	G	13	GENIC	homozygous	119821597
20	42968224	42968225	T	G	13	GENIC	homozygous	119821598
20	42968225	42968226	T	C	13	GENIC	homozygous	119821599
20	42968226	42968227	T	A	13	GENIC	homozygous	119821600
20	42968227	42968228	T	G	13	GENIC	homozygous	119821601
20	42968229	42968230	T	G	13	GENIC	homozygous	109270024
20	42968279	42968280	C	G	24	GENIC	possibly homozygous	109202864
20	42968319	42968320	T	C	25	GENIC	homozygous	109202866
20	42968327	42968328	C	T	24	GENIC	homozygous	109202868
20	42968405	42968406	T	C	37	GENIC	possibly homozygous	109202870
20	42968711	42968712	G	C	27	GENIC	possibly homozygous	109376378
20	42969526	42969527	A	G	66	GENIC	heterozygous	109202872
20	42969539	42969540	A	G	64	GENIC	homozygous	109202874