chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4126071066126071067CA42GENIChomozygous113301657
4126071221126071222AG39GENIChomozygous113301658
4126071344126071345GA36GENIChomozygous113301659
4126071658126071659CT49GENIChomozygous113301660
4126071718126071719AT37GENIChomozygous113301661
4126072108126072109GA36GENIChomozygous113301662
4126073519126073520GA21GENIChomozygous113301663
4126073821126073822AG45GENIChomozygous113301664
4126073983126073984CT33GENICpossibly homozygous113301665
4126074447126074448TC21GENIChomozygous113301666