chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
121334645313346454CT18GENIChomozygous115362625
121334740113347402AC25GENIChomozygous115260521
121334789513347896GC9GENIChomozygous115260523
121334791213347913TA11GENIChomozygous115260525
121334820313348204CG6GENIChomozygous115260527
121334870713348708CT7GENIChomozygous115260529
121334882113348822AT5GENIChomozygous115260531
121334912513349126GT15GENIChomozygous115260533
121335241213352413TC23GENIChomozygous115260535
121335247813352479CG20GENIChomozygous115260537
121335249613352497AG13GENIChomozygous115260539
121335385113353852AG27GENIChomozygous115260541
121335579413355795GA12GENIChomozygous115260545
121335623913356240TC20GENIChomozygous115260547
121335627013356271AG26GENIChomozygous115260549
121335743013357431AT22GENIChomozygous115260551
121335892613358927CT19GENIChomozygous115260553
121335933513359336CA27GENIChomozygous115260555
121336050513360506TC24GENIChomozygous115260557
121336065613360657GA14GENIChomozygous115260559
121336167413361675CT22GENIChomozygous115260561
121336432513364326AC11GENIChomozygous115260563
121336538513365386GT25GENIChomozygous115260565
121336601113366012GA26GENIChomozygous115260567
121336697913366980CT13GENIChomozygous115260569
121336721413367215GA22GENIChomozygous115260571