chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50736422	50736424	TC		21	GENIC	homozygous	129052840
13	50737801	50737802	G	A	52	GENIC	homozygous	114341432
13	50739841	50739842	T		49	GENIC	homozygous	129052841
13	50740771	50740772	G	A	24	GENIC	homozygous	118450664
13	50741229	50741230	C	T	56	GENIC	homozygous	114341434
13	50741895	50741896	A	G	53	GENIC	homozygous	114341436
13	50742038	50742039	C	T	39	GENIC	possibly homozygous	114341438
13	50742251	50742252	T	C	38	GENIC	homozygous	114341440
13	50742455	50742455		C	48	GENIC	homozygous	129052842
13	50744854	50744855	A	G	21	GENIC	homozygous	114341444
13	50745078	50745078		G	19	GENIC	homozygous	129052843
13	50745867	50745868	A	C	42	GENIC	homozygous	114341446
13	50746645	50746646	A	G	21	GENIC	homozygous	114341448
13	50739798	50739799	A	G	53	GENIC	homozygous	114549988
13	50747391	50747392	C	G	49	GENIC	homozygous	114341450
13	50748417	50748418	A	G	40	GENIC	possibly homozygous	114341452
13	50748493	50748494	A	G	38	GENIC	homozygous	114341454