chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5083496	5083497	G	A	24	GENIC	homozygous	109076576
20	5083564	5083565	T	C	30	GENIC	possibly homozygous	109076578
20	5083705	5083706	C	T	37	GENIC	homozygous	109076580
20	5084113	5084114	C	T	14	GENIC	homozygous	109076582
20	5084185	5084186	C	T	20	GENIC	homozygous	109076584
20	5084638	5084639	G	T	16	GENIC	homozygous	109076595
20	5083772	5083773	T	C	29	GENIC	homozygous	109233805
20	5083975	5083976	G	C	24	GENIC	homozygous	109329674
20	5084247	5084248	A	G	11	GENIC	homozygous	109076586
20	5084480	5084481	G	A	24	GENIC	homozygous	109076588
20	5084562	5084563	C	T	23	GENIC	homozygous	109076590
20	5084568	5084569	A	G	24	GENIC	homozygous	109076593
20	5084826	5084827	T	C	24	GENIC	homozygous	109076597
20	5084850	5084851	G	A	20	GENIC	homozygous	109076599
20	5084878	5084879	G	A	21	GENIC	homozygous	109076601
20	5084957	5084958	T	C	27	GENIC	homozygous	109076603