chr	start	stop	reference nuc	variant nuc	depth	genic status	zygosity	variant ID
14	17616390	17616391	C	T	18	GENIC	homozygous	113578070
14	17616500	17616501	G	A	22	GENIC	homozygous	113578071
14	17616969	17616970	T	A	20	GENIC	homozygous	113578072
14	17617742	17617743	C	A	21	GENIC	homozygous	113578073
14	17619228	17619229	T	A	28	GENIC	homozygous	113578074
14	17620908	17620909	G	A	19	GENIC	homozygous	113578075
14	17621382	17621383	T	C	35	GENIC	homozygous	113362772
14	17621514	17621515	C	T	39	GENIC	homozygous	113578076
14	17622199	17622200	C	T	30	GENIC	homozygous	113578077
14	17622565	17622566	T	A	25	GENIC	homozygous	113362774
14	17625259	17625260	G	A	34	GENIC	homozygous	113578078
14	17625421	17625422	A	C	22	GENIC	possibly homozygous	113578079
14	17625885	17625886	A	G	16	GENIC	homozygous	113362781
14	17627520	17627521	C	T	18	GENIC	homozygous	113578080
14	17629159	17629160	G	T	19	GENIC	homozygous	113578081
14	17630313	17630314	G	A	27	GENIC	homozygous	113578082
14	17630413	17630414	C	G	19	GENIC	homozygous	113578083