chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	14804844	14804846	CT		75	GENIC	homozygous	139380701
14	14805106	14805107	A	G	48	GENIC	homozygous	139456727
14	14805749	14805750	T	C	64	GENIC	homozygous	139456728
14	14805847	14805848	G	A	67	GENIC	homozygous	139456729
14	14806073	14806074	C	T	67	GENIC	homozygous	139456730
14	14806448	14806449	T	C	70	GENIC	possibly homozygous	139456731
14	14806959	14806960	G	A	62	GENIC	homozygous	139456732
14	14807489	14807490	A	G	59	GENIC	homozygous	139456733
14	14808481	14808482	C	T	52	GENIC	homozygous	139456734
14	14808633	14808634	C	T	52	GENIC	homozygous	139456735
14	14809315	14809316	C	A	66	GENIC	homozygous	139456736
14	14810331	14810332	T	C	54	GENIC	homozygous	139456737
14	14810357	14810359	AC		53	GENIC	homozygous	139380702
14	14810693	14810694	T	G	45	GENIC	homozygous	139456738
14	14811012	14811012		AAAC	33	GENIC	heterozygous	139380704
14	14811666	14811667	T	C	65	GENIC	homozygous	139456739
14	14811897	14811898	A	G	59	GENIC	homozygous	139456740
14	14812048	14812049	G	A	51	GENIC	homozygous	139456741
14	14812706	14812707	C	T	44	GENIC	homozygous	139456742
14	14812740	14812741	T	C	49	GENIC	homozygous	139456743