chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
83918119939181200GA26GENIChomozygous117104624
83918427239184273CT38GENIChomozygous117104626
83918453239184533GA30GENIChomozygous117104628
83918541839185419TC23GENIChomozygous116462202
83918587239185873TG29GENIChomozygous116462211
83918602639186027GT22GENIChomozygous116462215
83918696439186965AG36GENICpossibly homozygous116799762
83918775539187756GA22GENIChomozygous116799764
83918857139188572TC28GENIChomozygous116462239
83918913939189140AG24GENIChomozygous116799766
83918962939189630AT23GENIChomozygous117104630
83919056139190562TG32GENIChomozygous116462250
83919390839193909AG26GENIChomozygous116462275
83919462739194628TC40GENIChomozygous117104632
83919504139195042GA22GENIChomozygous117104634
83919619939196200GA24GENIChomozygous116799774
83919631739196318TA24GENIChomozygous117104636
83919728239197283GA19GENIChomozygous116799776
83919827039198271GA21GENIChomozygous116799778
83920115439201155GC28GENIChomozygous117104638
83920152039201521AC42GENIChomozygous116462343