chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	37266007	37266008	T	C	61	GENIC	homozygous	130422060
13	37271327	37271327		G	35	GENIC	homozygous	129043181
13	37271331	37271332	C		34	GENIC	homozygous	129043182
13	37271356	37271357	G		39	GENIC	homozygous	129043183
13	37271378	37271378		T	42	GENIC	homozygous	129043184
13	37271510	37271510		G	54	GENIC	homozygous	129043185
13	37271594	37271594		G	48	GENIC	homozygous	129043186
13	37271634	37271635	A		46	GENIC	homozygous	129043187
13	37271638	37271638		TG	45	GENIC	homozygous	129043188
13	37289507	37289508	G		51	GENIC	homozygous	129043192
13	37289535	37289536	T	C	42	GENIC	homozygous	114315654
13	37289536	37289537	T	A	40	GENIC	homozygous	114315655
13	37289537	37289538	T	G	40	GENIC	homozygous	114315656
13	37289542	37289543	C		40	GENIC	homozygous	129043193
13	37289548	37289549	G		39	GENIC	homozygous	129043194
13	37289552	37289553	G		38	GENIC	homozygous	129043195
13	37289638	37289639	C		33	GENIC	homozygous	129043196
13	37289671	37289672	A		29	GENIC	homozygous	129043197
13	37289695	37289696	T		34	GENIC	homozygous	129043198
13	37291697	37291697		T	44	GENIC	homozygous	129043201