chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	11609684	11609685	A	G	54	GENIC	homozygous	50278686
12	11609725	11609726	C	CTT	28	GENIC	homozygous	50278687
12	11609870	11609871	T	C	40	GENIC	homozygous	50278688
12	11611390	11611391	G	A	34	GENIC	homozygous	50278689
12	11612392	11612393	T	C	58	GENIC	possibly homozygous	50278690
12	11612536	11612537	C	G	63	GENIC	homozygous	50278691
12	11613068	11613069	A	G	54	GENIC	homozygous	50278692
12	11613393	11613394	A	G	50	GENIC	possibly homozygous	50278693
12	11613554	11613555	C	T	45	GENIC	homozygous	50278694
12	11613643	11613644	A	G	51	GENIC	homozygous	50278695
12	11613695	11613696	G	GC	19	GENIC	possibly homozygous	50050501