chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141005837210058373AG27GENIChomozygous986187557
141005839310058394AC26GENIChomozygous986187558
141005854510058546CA29GENIChomozygous986187559
141005889610058897GA17GENIChomozygous986187560
141006082010060821AG24GENIChomozygous986187561
141006091510060916TA28GENIChomozygous986187562
141006096610060967CT28GENIChomozygous986187563
141006108710061088GC20GENIChomozygous986187564
141006114010061141CT12GENIChomozygous986187565
141006114210061143AT12GENIChomozygous986187566
141006115310061154TC16GENIChomozygous986187567
141006119810061199GA28GENIChomozygous986187568
141006142010061421GA13GENIChomozygous986187569
141006142310061424TA12GENIChomozygous986187570
141006144610061447CA18GENIChomozygous986187571
141006157910061580AG26GENIChomozygous986187572
141006158510061586AG24GENIChomozygous986187573
141006159510061596GA24GENIChomozygous986187574
141006163110061632CT24GENIChomozygous986187575
141006187310061874GA18GENIChomozygous986187576
141006187510061876CA18GENIChomozygous986187577