chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	15232571	15232572	A	-	1	GENIC	homozygous	50071786
12	15232576	15232577	G	-	1	GENIC	homozygous	50071788
12	15232593	15232594	G	-	1	GENIC	homozygous	50071790
12	15232598	15232599	G	-	1	GENIC	homozygous	50071792
12	15232605	15232606	G	-	1	GENIC	homozygous	50071794
12	15232635	15232636	G	-	1	GENIC	homozygous	50071796
12	15232646	15232647	A	-	2	GENIC	homozygous	50071798
12	15232660	15232661	A	-	4	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	11	GENIC	homozygous	50071808
12	15233071	15233072	G	-	33	GENIC	homozygous	50071810
12	15233207	15233208	G	-	38	GENIC	homozygous	50071812
12	15236382	15236383	A	AGT	10	GENIC	possibly homozygous	50071815
12	15236618	15236619	C	T	31	GENIC	heterozygous	50071817
12	15236695	15236696	A	C	37	GENIC	heterozygous	50071819
12	15236707	15236708	A	-	19	GENIC	possibly homozygous	50071821
12	15237549	15237550	T	A	17	GENIC	heterozygous	50071823
12	15241356	15241358	AT	--	36	GENIC	heterozygous	50071825
12	15242138	15242139	T	C	34	GENIC	homozygous	50071827
12	15245224	15245246	TGGGTTAAGGGCACATGAGTGC	----------------------	14	GENIC	homozygous	50071829
12	15246073	15246074	T	C	22	GENIC	homozygous	50071831
12	15246133	15246134	C	T	24	GENIC	heterozygous	50071833
12	15246133	15246134	C	CGTGTGT	22	GENIC	homozygous	50071835
12	15247662	15247663	C	CG	17	GENIC	homozygous	50071837
12	15236706	15236708	AA	--	19	GENIC	heterozygous	50417863