chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139232325139232326CT52GENIChomozygous115936564
7139233126139233127CT61GENIChomozygous115936565
7139234792139234793TA43GENICpossibly homozygous115936566
7139234882139234883TA35GENIChomozygous115936567
7139235079139235080CT43GENIChomozygous115936568
7139235308139235309GA42GENIChomozygous115936569
7139236109139236110TC51GENIChomozygous115936570
7139236278139236279CT54GENIChomozygous115936571
7139237957139237958AG61GENIChomozygous115936572
7139237989139237990GA60GENIChomozygous115936573
7139233760139233760T39GENICpossibly homozygous128528501
7139235645139235645G45GENIChomozygous128528502
7139238432139238433T51GENIChomozygous128528503
7139239219139239220CT59GENIChomozygous115936574
7139239430139239431CT52GENIChomozygous115936575
7139239552139239553T44GENIChomozygous128528504
7139239637139239638GA52GENIChomozygous115936576
7139240021139240022CT42GENIChomozygous115936577
7139240451139240452CT42GENIChomozygous115936578
7139240825139240826AG48GENIChomozygous115936579
7139242115139242116AG71GENIChomozygous115936580
7139244709139244710GA46GENIChomozygous115936581
7139245867139245868TC61GENIChomozygous115936582
7139246149139246150CA47GENIChomozygous115936583
7139246396139246397CA45GENIChomozygous115936584
7139246453139246454GA42GENIChomozygous115936585
7139246501139246502AG47GENIChomozygous115936586
7139246721139246722TC51GENIChomozygous115936587
7139246894139246895TC50GENIChomozygous115936588
7139251080139251082GG43GENIChomozygous128528505
7139251109139251110GA41GENIChomozygous115936589
7139253260139253261GA20GENIChomozygous115936590
7139246414139246415AG41GENIChomozygous128563980