chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104508022645080227GA28GENIChomozygous51441695
104508295845082959GA26GENIChomozygous51441696
104508389345083894GGACCT22GENIChomozygous51441697
104508398745083988CT14GENIChomozygous51441698
104508414745084153CTCTCG------17GENIChomozygous51441699
104508545345085454G-31GENIChomozygous51441702
104508617845086179TA15GENIChomozygous51441703
104508630945086328TTTTTTTTTTTTTTTTTTT-------------------21GENICpossibly homozygous52372840
104508643345086434CCT13GENICheterozygous52372842
104508645545086456C-16GENICheterozygous52372844
104508664445086645CT25GENIChomozygous51441704
104508710445087105AAT24GENICpossibly homozygous51441705
104508802645088027TTG25GENIChomozygous51441706
104508844645088447CT22GENIChomozygous51441707
104508895645088957TC29GENIChomozygous51441708
104508905445089055CT33GENIChomozygous51441709
104508979945089800AG31GENIChomozygous51441710