chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5101556444101556445TC24GENIChomozygous113941749
5101557688101557689GA20GENIChomozygous113941751
5101558635101558636AG11GENIChomozygous113941753
5101559558101559559CT13GENIChomozygous113941755
5101563819101563820A17GENIChomozygous128218256
5101565326101565326G18GENIChomozygous128218257
5101568227101568228A19GENIChomozygous128218258
5101568713101568714AC20GENIChomozygous113941757
5101571224101571225GA23GENIChomozygous113941759
5101574084101574085CT20GENIChomozygous113941761
5101574332101574336TCAG16GENIChomozygous128218259
5101574872101574872ATAG22GENIChomozygous128218260
5101584519101584519T18GENIChomozygous128218261
5101585232101585233AG9GENICpossibly homozygous113941763
5101585371101585372GA26GENIChomozygous113941765
5101587363101587365TC13GENIChomozygous128218262