chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	15232635	15232636	G	-	1	GENIC	homozygous	50071796
12	15232646	15232647	A	-	3	GENIC	homozygous	50071798
12	15232660	15232661	A	-	3	GENIC	homozygous	50071800
12	15232679	15232680	G	T	5	GENIC	homozygous	50071802
12	15232688	15232689	G	-	5	GENIC	homozygous	50071804
12	15232695	15232696	G	-	7	GENIC	homozygous	50071806
12	15232706	15232707	G	GC	15	GENIC	homozygous	50071808
12	15233071	15233072	G	-	7	GENIC	heterozygous	50071810
12	15233207	15233208	G	-	27	GENIC	homozygous	50071812
12	15236382	15236383	A	AGT	4	GENIC	heterozygous	50071815
12	15236695	15236696	A	C	18	GENIC	homozygous	50071819
12	15236707	15236708	A	-	19	GENIC	homozygous	50071821
12	15241356	15241358	AT	--	18	GENIC	heterozygous	50071825
12	15242138	15242139	T	C	29	GENIC	homozygous	50071827
12	15244374	15244376	AA	--	7	GENIC	heterozygous	50560568
12	15245224	15245246	TGGGTTAAGGGCACATGAGTGC	----------------------	22	GENIC	homozygous	50071829
12	15246073	15246074	T	C	4	GENIC	homozygous	50071831
12	15247662	15247663	C	CG	31	GENIC	homozygous	50071837
12	15241357	15241358	T	C	18	GENIC	possibly homozygous	50533560
12	15244373	15244374	T	TA	7	GENIC	heterozygous	50533562
12	15248401	15248402	T	TAAAAAAAAAAAAAAAAA	12	GENIC	homozygous	50533564
12	15247659	15247660	C	G	32	GENIC	homozygous	50504018