chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121334645313346454CT26GENIChomozygous115362625
121334740113347402AC36GENIChomozygous115260521
121334789513347896GC31GENIChomozygous115260523
121334791213347913TA31GENIChomozygous115260525
121334820313348204CG25GENIChomozygous115260527
121334870713348708CT12GENIChomozygous115260529
121334882113348822AT23GENIChomozygous115260531
121334912513349126GT17GENIChomozygous115260533
121335241213352413TC28GENIChomozygous115260535
121335247813352479CG28GENIChomozygous115260537
121335249613352497AG27GENICpossibly homozygous115260539
121335385113353852AG27GENIChomozygous115260541
121335432313354324CT18GENIChomozygous115260543
121335579413355795GA25GENICpossibly homozygous115260545
121335623913356240TC14GENIChomozygous115260547
121335627013356271AG16GENIChomozygous115260549
121335743013357431AT18GENIChomozygous115260551
121335892613358927CT24GENIChomozygous115260553
121335933513359336CA37GENIChomozygous115260555
121336050513360506TC30GENIChomozygous115260557
121336065613360657GA18GENIChomozygous115260559
121336167413361675CT15GENIChomozygous115260561
121336432513364326AC18GENIChomozygous115260563
121336538513365386GT26GENIChomozygous115260565
121336601113366012GA20GENIChomozygous115260567
121336697913366980CT21GENIChomozygous115260569
121336721413367215GA16GENIChomozygous115260571