chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	31792697	31792698	G	T	26	GENIC	heterozygous	50421405
12	31792771	31792772	C	A	8	GENIC	heterozygous	50421406
12	31792784	31792785	T	C	3	GENIC	homozygous	50421407
12	31807074	31807075	C	T	25	GENIC	heterozygous	50411716
12	31808109	31808110	G	GT	7	GENIC	homozygous	50174512
12	31808113	31808114	A	C	5	GENIC	homozygous	50174513
12	31832863	31832864	C	CT	20	GENIC	heterozygous	50421408
12	31833164	31833165	G	GA	5	GENIC	heterozygous	50174516
12	31833165	31833166	A	-	5	GENIC	heterozygous	50174517
12	31841132	31841135	AAA	---	18	GENIC	heterozygous	50421409
12	31841427	31841428	C	A	22	GENIC	possibly homozygous	50174518
12	31843994	31843995	C	T	29	GENIC	heterozygous	50174519
12	31844020	31844021	G	A	27	GENIC	heterozygous	50174520
12	31844042	31844043	A	T	28	GENIC	heterozygous	50174521
12	31844590	31844591	A	C	12	GENIC	heterozygous	50174523
12	31844631	31844632	T	A	7	GENIC	homozygous	50174525
12	31844650	31844651	C	T	10	GENIC	possibly homozygous	50174526
12	31844651	31844652	G	T	10	GENIC	possibly homozygous	50174527
12	31844764	31844765	C	T	26	GENIC	heterozygous	50174528
12	31846856	31846857	A	G	32	GENIC	heterozygous	50174529
12	31844647	31844648	G	A	8	GENIC	homozygous	50312702
12	31844638	31844639	T	A	7	GENIC	homozygous	50312700