chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	8126538	8126539	G	C	55	GENIC	homozygous	139077548
12	8126627	8126628	G	T	49	GENIC	homozygous	139077549
12	8127033	8127034	C	T	76	GENIC	homozygous	139077550
12	8127336	8127336		A	51	GENIC	homozygous	139039272
12	8127337	8127338	G	C	52	GENIC	homozygous	139077551
12	8127339	8127345	GTTTGT		52	GENIC	homozygous	139039273
12	8127435	8127436	T	C	59	GENIC	homozygous	139077552
12	8129111	8129112	A	G	57	GENIC	homozygous	139077553
12	8129889	8129890	C	T	56	GENIC	homozygous	139077554
12	8130191	8130192	C	T	54	GENIC	homozygous	139077555
12	8131601	8131601		G	20	GENIC	possibly homozygous	139039274
12	8131632	8131633	T	A	17	GENIC	homozygous	139077556
12	8131986	8131987	A		38	GENIC	homozygous	139039275
12	8133514	8133515	A	T	71	GENIC	homozygous	139077557
12	8135421	8135422	A	G	56	GENIC	homozygous	139077558
12	8135915	8135916	A	G	56	GENIC	homozygous	139077559
12	8137369	8137370	T	C	51	GENIC	homozygous	139077560
12	8137824	8137825	G	A	49	GENIC	homozygous	139077561
12	8137914	8137915	A	G	61	GENIC	homozygous	139077562
12	8138824	8138825	C	T	40	GENIC	homozygous	139077563
12	8138829	8138830	C	T	41	GENIC	homozygous	139077564
12	8139147	8139148	G	A	62	GENIC	homozygous	139077565
12	8131690	8131691	A		8	GENIC	heterozygous	403315112
12	8131690	8131691	A	C	8	GENIC	homozygous	154756957