chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	5468601	5468602	G	A	38	GENIC	homozygous	109390310
20	5468795	5468796	A	T	33	GENIC	homozygous	109296945
20	5469183	5469184	C	T	29	GENIC	homozygous	109234075
20	5469497	5469498	A	G	17	GENIC	homozygous	109078098
20	5472093	5472094	G	A	28	GENIC	homozygous	109078106
20	5472889	5472890	C	T	42	GENIC	homozygous	109078108
20	5472898	5472899	T	C	46	GENIC	homozygous	109390311
20	5473992	5473993	T	C	30	GENIC	homozygous	109078112
20	5474167	5474168	G	T	36	GENIC	homozygous	109078114
20	5474203	5474204	G	A	34	GENIC	homozygous	109078116
20	5474304	5474305	C	A	29	GENIC	homozygous	109390312
20	5474526	5474527	A	G	29	GENIC	homozygous	109390313
20	5474740	5474741	G	C	31	GENIC	homozygous	109390314
20	5474743	5474744	C	T	33	GENIC	homozygous	109390315
20	5474781	5474782	C	A	28	GENIC	homozygous	109390316
20	5474870	5474871	G	T	32	GENIC	homozygous	109390317
20	5475846	5475847	A	G	17	GENIC	homozygous	109078118