chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1208477363208477364AG21GENIChomozygous108985272
1208477495208477496GT22GENIChomozygous109188497
1208477615208477616TC35GENIChomozygous108985273
1208477966208477967AT16GENIChomozygous108985277
1208477997208477998TC16GENIChomozygous108985278
1208478045208478046TC11GENIChomozygous109188501
1208478050208478051CT12GENIChomozygous109188503
1208478068208478069TA13GENIChomozygous120511744
1208478075208478076AC13GENIChomozygous109188505
1208478076208478077TC13GENIChomozygous109188507
1208478112208478113TC12GENIChomozygous109188509
1208478153208478154GA19GENIChomozygous108985279
1208478160208478161CT20GENIChomozygous109188511
1208478262208478263TC19GENIChomozygous109188513
1208478370208478371GA28GENIChomozygous108985280
1208478754208478755TC23GENIChomozygous108985281
1208478782208478783TC24GENIChomozygous108985282
1208478857208478858CT27GENIChomozygous108985283
1208478929208478930AG30GENIChomozygous108985284
1208478940208478941CA26GENIChomozygous108985285
1208481105208481106TC14GENIChomozygous108985295
1208481803208481804GA18GENIChomozygous109188515
1208482119208482120AG7GENIChomozygous108985298
1208482126208482127GA6GENIChomozygous108985299
1208482474208482475AC26GENIChomozygous108985300
1208483004208483005AG24GENIChomozygous109188517
1208483078208483079TC28GENIChomozygous109188519
1208484479208484480TC37GENIChomozygous108985302
1208484486208484487TC34GENIChomozygous108985303
1208490024208490025GA36GENIChomozygous109188527
1208491660208491661GA56GENIChomozygous108518359
1208493973208493974TG19GENIChomozygous108985323
1208495391208495392TC22GENIChomozygous109188529
1208498814208498815TC19GENIChomozygous109188531
1208499780208499781AG22GENIChomozygous120511745
1208499781208499782CA22GENIChomozygous120511746
1208500239208500240AG17GENIChomozygous108985325
1208500675208500676CG44GENIChomozygous108985326
1208501049208501050GA19GENIChomozygous109188533
1208501134208501135GA16GENIChomozygous108985327