chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
12	48105874	48105875	T	C	42	GENIC	homozygous	115345490
12	48106437	48106438	A	G	36	GENIC	homozygous	115345492
12	48106916	48106917	A	G	41	GENIC	homozygous	115345494
12	48106928	48106929	C	T	42	GENIC	homozygous	115345496
12	48107588	48107589	G	A	34	GENIC	homozygous	115345498
12	48109829	48109830	A	C	33	GENIC	homozygous	115345500
12	48110950	48110951	G	T	35	GENIC	homozygous	115345502
12	48111027	48111028	G	C	38	GENIC	homozygous	115345504
12	48112965	48112966	T	C	20	GENIC	homozygous	115345506
12	48114669	48114670	G	A	42	GENIC	homozygous	115345510
12	48116555	48116556	G	A	18	GENIC	homozygous	115345512
12	48117108	48117109	C	A	40	GENIC	homozygous	115345514
12	48117412	48117413	G	A	69	GENIC	heterozygous	118272944
12	48117459	48117460	C	A	67	GENIC	heterozygous	118272945
12	48119145	48119146	G	A	35	GENIC	homozygous	115345516
12	48121118	48121119	A	T	41	GENIC	homozygous	115345518