chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
152259295022592951CT16GENIChomozygous48255943
152259395522593956CT14GENICpossibly homozygous48255944
152259400522594006TC19GENICpossibly homozygous48255946
152259411822594119AG24GENICheterozygous48255947
152259423122594232AG23GENICpossibly homozygous48255949
152259449822594499CT19GENICheterozygous48255950
152259464022594641TC13GENICheterozygous48255952
152259467822594679CT14GENIChomozygous48255953
152259527522595276A-24GENIChomozygous48255961
152259539922595400CG22GENICpossibly homozygous48255962
152259544622595447GA21GENICheterozygous48742307
152259608922596090GGAGAGAGAC2GENIChomozygous48255966
152259609622596097TA2GENIChomozygous48255968
152259610522596106GC2GENIChomozygous48255969
152259611022596111GGT3GENIChomozygous48255971
152259644922596450CT23GENICheterozygous48255972
152259707822597079CA18GENIChomozygous48255974
152259899522598996AG29GENIChomozygous48255975
152260140822601409TC2GENIChomozygous48255978
152260170322601704TC16GENICpossibly homozygous48255980