chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104526226045262261CT24GENIChomozygous51442112
104526238945262390GA27GENIChomozygous51442114
104526247945262480TG27GENIChomozygous51442115
104526273745262738CT17GENIChomozygous51442116
104526331645263317AG7GENIChomozygous51442117
104526501945265020AG15GENIChomozygous51442118
104526712445267128TTTT----7GENICheterozygous51442119
104526712545267128TTT---7GENICheterozygous51442120
104526714445267145TA14GENIChomozygous52317945
104526726345267266AAC---26GENIChomozygous51873176
104526802045268021GA13GENIChomozygous51442121
104526899045268991CT32GENIChomozygous51442122
104526936145269362AG2GENIChomozygous51442129
104526957945269580TA30GENIChomozygous51442130
104527044945270450GA23GENIChomozygous51442131