chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1208477363208477364AG27GENIChomozygous108985272
1208477495208477496GT22GENIChomozygous109188497
1208477615208477616TC21GENIChomozygous108985273
1208477966208477967AT14GENIChomozygous108985277
1208477997208477998TC15GENIChomozygous108985278
1208478045208478046TC16GENIChomozygous109188501
1208478050208478051CT16GENIChomozygous109188503
1208478068208478069TA18GENIChomozygous120511744
1208478075208478076AC17GENIChomozygous109188505
1208478076208478077TC18GENIChomozygous109188507
1208478112208478113TC13GENIChomozygous109188509
1208478153208478154GA12GENIChomozygous108985279
1208478160208478161CT13GENIChomozygous109188511
1208478262208478263TC19GENIChomozygous109188513
1208478370208478371GA19GENIChomozygous108985280
1208478754208478755TC31GENIChomozygous108985281
1208478782208478783TC35GENIChomozygous108985282
1208478857208478858CT32GENIChomozygous108985283
1208478929208478930AG25GENIChomozygous108985284
1208478940208478941CA22GENIChomozygous108985285
1208481803208481804GA27GENIChomozygous109188515
1208482474208482475AC10GENIChomozygous108985300
1208483004208483005AG28GENIChomozygous109188517
1208483078208483079TC20GENIChomozygous109188519
1208484479208484480TC30GENIChomozygous108985302
1208484486208484487TC30GENIChomozygous108985303
1208490024208490025GA22GENIChomozygous109188527
1208493973208493974TG19GENIChomozygous108985323
1208495391208495392TC19GENIChomozygous109188529
1208498814208498815TC29GENIChomozygous109188531
1208499780208499781AG26GENIChomozygous120511745
1208499781208499782CA26GENIChomozygous120511746
1208500239208500240AG20GENIChomozygous108985325
1208500675208500676CG42GENIChomozygous108985326
1208501049208501050GA29GENIChomozygous109188533
1208501134208501135GA26GENIChomozygous108985327