chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121273952712739528GA27GENIChomozygous115259063
121273978012739781TA18GENIChomozygous115259065
121273986712739868TC23GENIChomozygous115259067
121273992312739924CT21GENIChomozygous115259069
121274181312741814TC20GENIChomozygous115259071
121274182312741824TC18GENIChomozygous115259073
121274204712742048AG19GENIChomozygous115259075
121274322912743230TC23GENIChomozygous115259077
121274326412743265AG21GENIChomozygous115259079
121274344112743442GC19GENIChomozygous115259081
121274445712744458CT11GENIChomozygous115259083
121274449912744500GA17GENIChomozygous115259085
121274654512746546GA17GENIChomozygous115259087