chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
20	13136205	13136206	G	A	33	GENIC	homozygous	109606241
20	13136207	13136208	A	G	33	GENIC	homozygous	109606243
20	13136215	13136216	C		34	GENIC	homozygous	129661072
20	13136220	13136221	A	T	32	GENIC	homozygous	109606246
20	13136243	13136245	CG		33	GENIC	homozygous	129661073
20	13136249	13136250	C		33	GENIC	homozygous	129661074
20	13136252	13136253	G		33	GENIC	homozygous	129661075
20	13136258	13136259	C		32	GENIC	homozygous	129661076
20	13136267	13136268	A	T	32	GENIC	homozygous	119769367
20	13136274	13136274		T	31	GENIC	homozygous	129661077
20	13136281	13136281		G	31	GENIC	homozygous	129661078
20	13136298	13136299	C		29	GENIC	homozygous	129661079
20	13136305	13136306	C		27	GENIC	homozygous	129661080
20	13136308	13136308		G	29	GENIC	homozygous	129661081
20	13136311	13136314	CTA		28	GENIC	homozygous	129661082
20	13138363	13138364	T		16	GENIC	homozygous	129661083
20	13138369	13138370	G		16	GENIC	homozygous	129661084
20	13138375	13138375		G	16	GENIC	homozygous	129661085
20	13138378	13138379	C	A	15	GENIC	homozygous	109099788
20	13138383	13138384	C	T	15	GENIC	homozygous	109372063
20	13138387	13138388	A	G	15	GENIC	homozygous	109372065
20	13138397	13138397		G	15	GENIC	homozygous	129661086
20	13138403	13138403		G	15	GENIC	homozygous	129661087
20	13138407	13138408	A		18	GENIC	homozygous	129661088