chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69946858499468585TC32GENICpossibly homozygous114915732
69946994699469947AG33GENIChomozygous114915733
69947025799470258TC16GENICheterozygous114915734
69947100199471002CT30GENIChomozygous114915735
69947155799471558CG15GENIChomozygous114915736
69947183999471840GA26GENIChomozygous114915737
69947308699473087AG36GENIChomozygous114915738
69947350799473508TC27GENIChomozygous114915739
69947488999474890CG22GENIChomozygous114915740
69947489599474896TA22GENIChomozygous114915741
69947496199474962TG24GENIChomozygous114915742