chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7120393432120393433GA42GENIChomozygous115856040
7120394124120394125TC49GENIChomozygous115856042
7120394877120394878AG59GENIChomozygous115856044
7120395692120395693CT50GENIChomozygous115856046
7120395790120395791AG62GENIChomozygous115856048
7120395896120395897AG42GENIChomozygous115856050
7120396479120396480AG45GENIChomozygous115856052
7120396518120396519GA56GENIChomozygous115856054
7120396571120396572GC61GENIChomozygous115856056
7120397035120397036CT65GENIChomozygous115856058
7120397110120397111TC61GENIChomozygous115856060
7120397353120397354AG58GENIChomozygous115856062
7120397963120397964AG52GENIChomozygous115856064
7120398405120398406GA59GENIChomozygous115856066
7120398897120398898CT45GENICpossibly homozygous115856068
7120399932120399933TC45GENIChomozygous115856070
7120400980120400981TC32GENIChomozygous115856072
7120401106120401107TC31GENIChomozygous115856074
7120401127120401128TG22GENIChomozygous115856076
7120401624120401625TC32GENIChomozygous115856078