chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
13	50090492	50090494	GT	--	28	GENIC	heterozygous	50601901
13	50097348	50097349	G	GTGTGTGTGTATGTGTGTGTGCATGTTTGTGTGTCTGTGTGTATGTTTGTGTATGTGTATGTGTGAGTGTGTGAGTGTGTGTGTGTGTGCATGTTTGTGTGTCTGTGTGTATGTTTGTGTATGTGTGTGTATGTGTGCATTTTTGTGGGTCTGTGTGTATGTTTGTGTATGTGTGAGTGTGTGTGTATGTGTGTGTGCATGTTTGTGTGTCTGTGTGTATGTTTGTGTA	16	GENIC	possibly homozygous	50517579
13	50106753	50106754	G	GT	23	GENIC	homozygous	49755372
13	50106773	50106828	CCCCCCCCCCAGGGAACTTCCCCCTTTGGGGGTGTAACCATTCCCCAGGGCAGGC	-------------------------------------------------------	23	GENIC	homozygous	50517580
13	50106837	50106838	C	G	7	GENIC	homozygous	49755378
13	50106840	50106841	C	A	8	GENIC	homozygous	49755379
13	50106850	50106851	G	-	9	GENIC	homozygous	49755380
13	50106856	50106857	C	-	10	GENIC	homozygous	49755381
13	50106862	50106863	C	-	10	GENIC	homozygous	49755382
13	50106870	50106871	T	-	11	GENIC	homozygous	49755383
13	50106875	50106876	C	A	11	GENIC	homozygous	50517581
13	50106876	50106877	G	C	11	GENIC	homozygous	50517582
13	50106883	50106884	A	T	15	GENIC	homozygous	49755384
13	50106896	50106897	G	-	19	GENIC	homozygous	49755385
13	50106907	50106908	G	T	22	GENIC	homozygous	49755386
13	50106909	50106910	A	-	23	GENIC	homozygous	49755387
13	50120532	50120533	G	GA	4	GENIC	heterozygous	50517585
13	50123500	50123504	TATC	----	10	GENIC	homozygous	49755395