chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120393432120393433GA39GENIChomozygous115856040
7120394124120394125TC35GENIChomozygous115856042
7120394877120394878AG41GENIChomozygous115856044
7120395692120395693CT31GENIChomozygous115856046
7120395790120395791AG30GENIChomozygous115856048
7120395896120395897AG35GENIChomozygous115856050
7120396479120396480AG39GENIChomozygous115856052
7120396571120396572GC31GENIChomozygous115856056
7120396700120396701CT34GENIChomozygous116409448
7120397035120397036CT36GENIChomozygous115856058
7120397110120397111TC26GENICpossibly homozygous115856060
7120397353120397354AG32GENIChomozygous115856062
7120397963120397964AG16GENIChomozygous115856064
7120398405120398406GA31GENIChomozygous115856066
7120398897120398898CT33GENIChomozygous115856068
7120399459120399460GA27GENIChomozygous116409449
7120399932120399933TC29GENIChomozygous115856070
7120400980120400981TC14GENIChomozygous115856072
7120401106120401107TC10GENIChomozygous115856074
7120401127120401128TG5GENIChomozygous115856076
7120401624120401625TC24GENIChomozygous115856078