chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
389835598983560CT8GENIChomozygous949346697
389838728983873TA12GENIChomozygous949346698
389840348984035CT15GENIChomozygous949346699
389843058984306TA6GENIChomozygous949346700
389846318984632CT11GENIChomozygous949346701
389847268984727TC14GENIChomozygous949346702
389847288984729GA15GENIChomozygous949346703
389849628984963GA9GENIChomozygous949346704
389850108985011CT6GENIChomozygous949346705
389850278985028AG6GENIChomozygous949346706
389850748985075GA7GENIChomozygous949346707
389863498986350CA23GENIChomozygous949346708
389870278987028GC17GENIChomozygous949346709
389887368988737GA15GENIChomozygous949346710
389893458989346TC23GENIChomozygous949346711
389903258990326TC17GENIChomozygous949346712
389914098991410TC17GENIChomozygous949346713
389921188992119TC7GENIChomozygous949346714
389923788992379AG14GENIChomozygous949346715
389926378992638AG16GENIChomozygous949346716
389930228993023CT17GENIChomozygous949346717
389951688995169GT3GENIChomozygous949346718
389951748995175TG2GENIChomozygous949346719
389958388995839GA13GENIChomozygous949346720
389973408997341AG19GENIChomozygous949346721
389982388998239CT14GENIChomozygous949346722
389984358998436TC12GENIChomozygous949346723
389985448998545AG12GENICheterozygous949346724
390029759002976CT7GENIChomozygous949346725
390034199003420GA8GENIChomozygous949346726
390064169006417CT7GENICheterozygous949346727
390065329006533TC11GENIChomozygous949346728
390067139006714CT10GENIChomozygous949346729
390080249008025CT11GENIChomozygous949346730
390094699009470AG14GENIChomozygous949346731
390123439012344CT12GENIChomozygous949346732