chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50736373	50736377	CTCT		17	GENIC	heterozygous	130106687
13	50736397	50736398	G	C	15	GENIC	heterozygous	118450662
13	50736422	50736424	TC		16	GENIC	possibly homozygous	129052840
13	50736435	50736437	TC		17	GENIC	heterozygous	130106689
13	50739841	50739842	T		15	GENIC	homozygous	129052841
13	50740771	50740772	G	A	19	GENIC	homozygous	118450664
13	50742455	50742455		C	21	GENIC	homozygous	129052842
13	50742740	50742741	G	A	17	GENIC	homozygous	114341442
13	50737801	50737802	G	A	26	GENIC	homozygous	114341432
13	50741229	50741230	C	T	15	GENIC	homozygous	114341434
13	50741895	50741896	A	G	13	GENIC	homozygous	114341436
13	50742038	50742039	C	T	17	GENIC	homozygous	114341438
13	50742251	50742252	T	C	20	GENIC	homozygous	114341440
13	50739798	50739799	A	G	17	GENIC	homozygous	114549988
13	50744854	50744855	A	G	10	GENIC	homozygous	114341444
13	50745078	50745078		G	5	GENIC	homozygous	129052843
13	50745867	50745868	A	C	24	GENIC	homozygous	114341446
13	50746645	50746646	A	G	10	GENIC	homozygous	114341448
13	50747391	50747392	C	G	19	GENIC	homozygous	114341450
13	50748417	50748418	A	G	26	GENIC	homozygous	114341452
13	50748493	50748494	A	G	22	GENIC	homozygous	114341454