chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
134937651649376518TG23GENICheterozygous132171775
134938231749382318C14GENICheterozygous129052227
134943464549434646CT59GENIChomozygous114337996
134945411549454116T36GENIChomozygous129052228
134945412349454124GC37GENIChomozygous114337998
134945412549454126TC37GENIChomozygous114338000
134945413249454133CA35GENIChomozygous114338002
134945413449454135G35GENIChomozygous129052229
134945413949454140TC36GENIChomozygous114338004
134945417849454179C36GENIChomozygous129052230
134945419349454194T38GENIChomozygous129052231
134945419749454198AC38GENIChomozygous114338006
134945421149454212T37GENIChomozygous129052232
134945421749454218T39GENIChomozygous129052233
134947995549479956GT40GENICheterozygous131138205
134948021049480211TG50GENICheterozygous130692521
134948024849480249CT42GENICheterozygous130692522
134948025149480252AG42GENICheterozygous130692523
134948025449480255CT42GENICheterozygous130692524
134948049649480497GA70GENICheterozygous130692525
134948051649480517GA72GENICheterozygous123731304
134948053049480531GA73GENICheterozygous129109151
134948065849480659TC54GENICheterozygous129109154
134948132049481321CG45GENICheterozygous123731323
134948154749481548CG53GENICheterozygous123731327
134948216349482164GA40GENICheterozygous131724496
134948216849482169AT41GENICheterozygous131724497
134948220449482205TC42GENICheterozygous130587044
134949389449493895GA16GENICheterozygous129109179