chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	1876193	1876194	T	C	44	GENIC	homozygous	109065121
20	1876408	1876409	A	T	44	GENIC	homozygous	109065123
20	1876430	1876431	A	G	39	GENIC	homozygous	109065125
20	1876595	1876596	G	A	35	GENIC	homozygous	109065127
20	1876761	1876762	T	C	38	GENIC	homozygous	109065129
20	1877105	1877106	T	C	52	GENIC	homozygous	109065131
20	1877129	1877130	T	C	62	GENIC	homozygous	109065133
20	1877158	1877159	T	C	66	GENIC	homozygous	109065135
20	1877389	1877390	C	T	42	GENIC	homozygous	109065137
20	1877396	1877397	T	C	40	GENIC	homozygous	109065139
20	1877416	1877417	A	G	41	GENIC	homozygous	109065141
20	1877423	1877424	A	G	40	GENIC	possibly homozygous	109065143
20	1877456	1877457	G	A	39	GENIC	homozygous	109065145
20	1877462	1877463	T	C	41	GENIC	homozygous	109065147
20	1877638	1877639	G	T	49	GENIC	heterozygous	109065149
20	1877756	1877757	A	G	41	GENIC	homozygous	109065151
20	1877946	1877947	G	A	38	GENIC	homozygous	109065153
20	1877950	1877951	T	C	39	GENIC	homozygous	109065155