chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50097345	50097346	T	TATG	35	GENIC	heterozygous	49755363
13	50097346	50097347	G	-	35	GENIC	heterozygous	49755364
13	50097348	50097363	GTGTGTGTGTATGGT	---------------	28	GENIC	heterozygous	49755365
13	50097348	50097349	G	-	28	GENIC	heterozygous	49755366
13	50097360	50097361	G	-	34	GENIC	heterozygous	49755367
13	50097360	50097361	G	GT	35	GENIC	heterozygous	49755368
13	50097417	50097418	G	GT	38	GENIC	heterozygous	49755370
13	50097588	50097589	A	AT	13	GENIC	heterozygous	49755371
13	50099789	50099790	A	-	32	GENIC	heterozygous	49946992
13	50106753	50106754	G	GT	18	GENIC	homozygous	49755372
13	50106787	50106788	A	-	1	GENIC	homozygous	49755373
13	50106809	50106811	AC	--	3	GENIC	homozygous	49755375
13	50106827	50106828	C	-	5	GENIC	homozygous	49755377
13	50106850	50106851	G	-	5	GENIC	homozygous	49755380
13	50106856	50106857	C	-	5	GENIC	homozygous	49755381
13	50106862	50106863	C	-	6	GENIC	homozygous	49755382
13	50106870	50106871	T	-	6	GENIC	homozygous	49755383
13	50106896	50106897	G	-	8	GENIC	homozygous	49755385
13	50106907	50106908	G	T	12	GENIC	homozygous	49755386
13	50106909	50106910	A	-	12	GENIC	homozygous	49755387
13	50106923	50106924	T	-	14	GENIC	homozygous	49755388
13	50106932	50106933	A	-	16	GENIC	homozygous	49755389
13	50106953	50106954	G	-	13	GENIC	homozygous	49755390
13	50106966	50106967	A	-	17	GENIC	homozygous	49755391
13	50116001	50116002	G	GA	9	GENIC	heterozygous	49946993
13	50119170	50119171	T	TAG	3	GENIC	homozygous	49755392
13	50120534	50120535	C	A	35	GENIC	possibly homozygous	49755393