chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8132446320132446321GA47GENIChomozygous116905018
8132449392132449393AG24GENICheterozygous116905022
8132449396132449397AG25GENICheterozygous116905024
8132449400132449401AG25GENICheterozygous116905026
8132451436132451437CG21GENIChomozygous116905028
8132453012132453013AG39GENIChomozygous116729594
8132456202132456203TG46GENIChomozygous116905030
8132459374132459375CG43GENIChomozygous116729597
8132459938132459939AG52GENIChomozygous116729599
8132460966132460967GA36GENICheterozygous117176442
8132462153132462154AG64GENIChomozygous116905032
8132466163132466164GA55GENICheterozygous117129312
8132468548132468549TC59GENIChomozygous116729604
8132469043132469044AG54GENICheterozygous117176443
8132469262132469263TC51GENIChomozygous116729606
8132469305132469306AT49GENICpossibly homozygous116905034
8132469309132469310TG50GENICpossibly homozygous116905036
8132469359132469360TG52GENIChomozygous116905038
8132469364132469365AC55GENICpossibly homozygous116905040
8132469424132469425AG47GENIChomozygous116905042
8132469467132469468CT33GENIChomozygous116905044
8132469624132469625TA42GENICpossibly homozygous116905046
8132479551132479552GA57GENIChomozygous116905048
8132483854132483855AG44GENIChomozygous116905050
8132495615132495616GT46GENIChomozygous116905052
8132496430132496431AG58GENIChomozygous116729617
8132497785132497786AG7GENICheterozygous116905054
8132500131132500132AG43GENIChomozygous116729619
8132503983132503984CT30GENIChomozygous116905056
8132504088132504089GT28GENIChomozygous116905058
8132504791132504792TG51GENICheterozygous117176444
8132513006132513007TC40GENIChomozygous116729624
8132513073132513074TG44GENIChomozygous116729625
8132514904132514905GA51GENIChomozygous116905062
8132515895132515896CT37GENIChomozygous116905064
8132517744132517745TG40GENIChomozygous116729627
8132523255132523256AG48GENIChomozygous116905066
8132532457132532458TG49GENIChomozygous116729632
8132535100132535101GT42GENICpossibly homozygous116905068