chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
10110139140110139141A-5GENIChomozygous51601058
10110139500110139501CT16GENIChomozygous51601059
10110140004110140007AAA---13GENIChomozygous51601060
10110140015110140019AAAT----15GENICpossibly homozygous51601061
10110140154110140155AG11GENIChomozygous51601062
10110140346110140347A-11GENIChomozygous51601063
10110140635110140636AG20GENIChomozygous51601064
10110140738110140739GA32GENIChomozygous51601065
10110140784110140785GT29GENIChomozygous51601066
10110142723110142725AA--10INTERGENIChomozygous51601067
10110142859110142860TC18INTERGENIChomozygous51601068
10110145666110145667TC26GENIChomozygous51601069
10110146190110146191AG22GENIChomozygous51601070
10110147003110147004TTG5GENIChomozygous51601071
10110147010110147011C-8GENICheterozygous51601072
10110147331110147332GA14GENICpossibly homozygous51601073
10110147657110147658CA16GENIChomozygous51601074
10110147827110147828AC27GENIChomozygous51601075