chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
69946858499468585TC32GENICpossibly homozygous812364993
69946994699469947AG33GENIChomozygous812364994
69947025799470258TC16GENICheterozygous812364995
69947100199471002CT30GENIChomozygous812364996
69947155799471558CG15GENIChomozygous812364997
69947183999471840GA26GENIChomozygous812364998
69947308699473087AG36GENIChomozygous812364999
69947350799473508TC27GENIChomozygous812365000
69947488999474890CG22GENIChomozygous812365001
69947489599474896TA22GENIChomozygous812365002
69947496199474962TG24GENIChomozygous812365003