chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1152020622152020623CT19GENICheterozygous153811349
1152020622152020623C19GENICpossibly homozygous403798382
1152020624152020625CT19GENICheterozygous153811350
1152020624152020625C19GENICpossibly homozygous403798383
1152020626152020627C19GENICpossibly homozygous403798384
1152020626152020627CT19GENICheterozygous403798385
1152020628152020629CT17GENIChomozygous141263021
1152020628152020629C19GENICheterozygous403798386
1152020630152020631CT21GENIChomozygous141263022
1152020630152020631C21GENICheterozygous403798387
1152020677152020678A14GENICheterozygous402968263
1152020677152020678AG14GENIChomozygous402968264
1152025668152025669TG52GENIChomozygous135710187
1152028118152028119CG58GENIChomozygous135710192
1152031179152031180AC49GENIChomozygous135710200
1152031478152031479TG57GENIChomozygous135710201
1152033790152033791GA51GENIChomozygous141263023
1152035943152035944AG53GENIChomozygous141263024
1152031176152031178TA49GENIChomozygous135437546
1152037052152037053CT46GENIChomozygous135710205