chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110139500110139501CT25GENICpossibly homozygous51601059
10110140004110140007AAA---2GENIChomozygous51601060
10110140154110140155AG24GENIChomozygous51601062
10110140346110140347A-21GENICheterozygous51601063
10110140635110140636AG10GENIChomozygous51601064
10110140738110140739GA22GENIChomozygous51601065
10110140784110140785GT11GENICheterozygous51601066
10110142723110142725AA--1INTERGENIChomozygous51601067
10110142859110142860TC12INTERGENICpossibly homozygous51601068
10110145666110145667TC21GENIChomozygous51601069
10110146190110146191AG20GENIChomozygous51601070
10110147331110147332GA28GENIChomozygous51601073
10110147657110147658CA17GENICpossibly homozygous51601074
10110147827110147828AC28GENICpossibly homozygous51601075