chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7139232325139232326CT17GENIChomozygous115936564
7139233126139233127CT22GENIChomozygous115936565
7139233760139233760T18GENIChomozygous128528501
7139234792139234793TA14GENIChomozygous115936566
7139234882139234883TA34GENIChomozygous115936567
7139235079139235080CT18GENIChomozygous115936568
7139235308139235309GA17GENIChomozygous115936569
7139235645139235645G15GENIChomozygous128528502
7139236109139236110TC23GENIChomozygous115936570
7139236278139236279CT23GENIChomozygous115936571
7139237957139237958AG18GENIChomozygous115936572
7139237989139237990GA15GENIChomozygous115936573
7139238432139238433T14GENIChomozygous128528503
7139239219139239220CT18GENIChomozygous115936574
7139239430139239431CT18GENIChomozygous115936575
7139239552139239553T17GENIChomozygous128528504
7139239637139239638GA12GENIChomozygous115936576
7139240021139240022CT18GENIChomozygous115936577
7139240451139240452CT16GENIChomozygous115936578
7139244709139244710GA22GENIChomozygous115936581
7139240825139240826AG14GENIChomozygous115936579
7139242115139242116AG18GENIChomozygous115936580
7139245867139245868TC17GENIChomozygous115936582
7139246149139246150CA23GENICpossibly homozygous115936583
7139246396139246397CA11GENIChomozygous115936584
7139246453139246454GA19GENIChomozygous115936585
7139246501139246502AG24GENIChomozygous115936586
7139246721139246722TC24GENIChomozygous115936587
7139246894139246895TC20GENIChomozygous115936588
7139251080139251082GG22GENIChomozygous128528505
7139251109139251110GA21GENIChomozygous115936589
7139253260139253261GA7GENIChomozygous115936590
7139246414139246415AG13GENIChomozygous128563980