chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5101556444101556445TC15GENIChomozygous113941749
5101557688101557689GA26GENIChomozygous113941751
5101558635101558636AG17GENIChomozygous113941753
5101559558101559559CT15GENIChomozygous113941755
5101568227101568228A24GENIChomozygous128218258
5101563819101563820A18GENIChomozygous128218256
5101565326101565326G16GENIChomozygous128218257
5101568713101568714AC27GENIChomozygous113941757
5101571224101571225GA19GENIChomozygous113941759
5101574084101574085CT18GENIChomozygous113941761
5101574332101574336TCAG7GENIChomozygous128218259
5101574872101574872ATAG20GENIChomozygous128218260
5101581410101581410G1GENIChomozygous133619546
5101584519101584519T9GENICpossibly homozygous128218261
5101585232101585233AG12GENIChomozygous113941763
5101585371101585372GA22GENIChomozygous113941765
5101587363101587365TC19GENIChomozygous128218262