chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
62709557827095579CT15GENIChomozygous115494074
62709582927095833TCTC24GENIChomozygous131660528
62709585127095852TG19GENIChomozygous115494076
62709588727095888CT22GENIChomozygous115494078
62709601827096030AGGAAGTTGAAT15GENIChomozygous131660529
62709618727096188GA17GENIChomozygous115494080
62709645527096456AG29GENIChomozygous115494082
62709735927097360CT29GENIChomozygous115494084
62709901227099013AG21GENIChomozygous115494086
62710251327102514GT21GENIChomozygous118571520
62710240927102409C26GENIChomozygous128325010
62710249627102498AA22GENIChomozygous128325011
62710250227102502CT22GENIChomozygous128325012
62710249927102500GA21GENIChomozygous118571518
62710250427102505GA22GENIChomozygous118571519
62710252127102522GT17GENIChomozygous118571521
62710252327102524GT17GENIChomozygous118571522
62710253127102533TA16GENIChomozygous128325013
62710253527102535CC16GENIChomozygous128325014
62710253627102537AC16GENIChomozygous118571523
62710253827102539AT14GENIChomozygous118571524
62710254127102542CT15GENIChomozygous118571525
62710254327102544GC15GENIChomozygous118571526
62710254927102550AT14GENIChomozygous118552806
62710255127102552GC13GENIChomozygous118571527
62710254827102549GC14GENIChomozygous118793071
62710252827102529AC16GENIChomozygous118690378