chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	1876193	1876194	T	C	29	GENIC	homozygous	109065121
20	1876354	1876355	T	G	32	GENIC	homozygous	109489654
20	1876408	1876409	A	T	28	GENIC	homozygous	109065123
20	1876430	1876431	A	G	29	GENIC	homozygous	109065125
20	1876595	1876596	G	A	37	GENIC	homozygous	109065127
20	1876761	1876762	T	C	40	GENIC	homozygous	109065129
20	1877105	1877106	T	C	15	GENIC	homozygous	109065131
20	1877129	1877130	T	C	16	GENIC	homozygous	109065133
20	1877158	1877159	T	C	17	GENIC	homozygous	109065135
20	1877389	1877390	C	T	26	GENIC	homozygous	109065137
20	1877396	1877397	T	C	24	GENIC	homozygous	109065139
20	1877416	1877417	A	G	29	GENIC	homozygous	109065141
20	1877423	1877424	A	G	30	GENIC	homozygous	109065143
20	1877456	1877457	G	A	25	GENIC	homozygous	109065145
20	1877462	1877463	T	C	24	GENIC	homozygous	109065147
20	1877638	1877639	G	T	28	GENIC	homozygous	109065149
20	1877756	1877757	A	G	30	GENIC	homozygous	109065151
20	1877946	1877947	G	A	26	GENIC	homozygous	109065153
20	1877950	1877951	T	C	29	GENIC	homozygous	109065155