chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	31808109	31808110	G	GT	11	GENIC	homozygous	50174512
12	31808113	31808114	A	C	10	GENIC	homozygous	50174513
12	31818862	31818863	C	CA	18	GENIC	heterozygous	50174514
12	31818863	31818864	A	-	18	GENIC	heterozygous	50174515
12	31833164	31833165	G	GA	24	GENIC	heterozygous	50174516
12	31833165	31833166	A	-	24	GENIC	heterozygous	50174517
12	31841427	31841428	C	A	28	GENIC	possibly homozygous	50174518
12	31844020	31844021	G	A	27	GENIC	heterozygous	50174520
12	31844042	31844043	A	T	16	GENIC	heterozygous	50174521
12	31844164	31844165	G	-	20	GENIC	heterozygous	50174522
12	31844590	31844591	A	C	5	GENIC	heterozygous	50174523
12	31844594	31844595	A	C	7	GENIC	heterozygous	50174524
12	31844631	31844632	T	A	10	GENIC	homozygous	50174525
12	31844638	31844639	T	A	8	GENIC	homozygous	50312700
12	31844647	31844648	G	A	8	GENIC	homozygous	50312702
12	31844650	31844651	C	T	9	GENIC	homozygous	50174526
12	31844651	31844652	G	T	11	GENIC	homozygous	50174527
12	31844764	31844765	C	T	34	GENIC	heterozygous	50174528
12	31846856	31846857	A	G	17	GENIC	heterozygous	50174529