chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50737919	50737920	G	T	28	GENIC	homozygous	115182316
13	50738428	50738429	C	T	37	GENIC	homozygous	115182318
13	50738917	50738918	G	A	35	GENIC	homozygous	114762406
13	50739798	50739799	A	G	22	GENIC	homozygous	114549988
13	50740941	50740942	C	A	13	GENIC	homozygous	114762408
13	50741784	50741785	C	T	25	GENIC	possibly homozygous	114762410
13	50741895	50741896	A	G	27	GENIC	homozygous	114341436
13	50742251	50742252	T	C	18	GENIC	homozygous	114341440
13	50743167	50743168	G	A	32	GENIC	possibly homozygous	114762412
13	50745867	50745868	A	C	37	GENIC	homozygous	114341446
13	50746645	50746646	A	G	23	GENIC	homozygous	114341448
13	50746885	50746886	A	C	25	GENIC	possibly homozygous	114762414
13	50747066	50747067	C	T	32	GENIC	possibly homozygous	114762416
13	50747153	50747154	G	A	29	GENIC	homozygous	114762418
13	50747391	50747392	C	G	23	GENIC	homozygous	114341450
13	50747644	50747645	A	G	7	GENIC	homozygous	114762420
13	50748078	50748079	G	T	23	GENIC	possibly homozygous	114762422
13	50748417	50748418	A	G	22	GENIC	homozygous	114341452