chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1266866964266866965TG15GENIChomozygous965888416
1266867306266867307GA34GENIChomozygous965888417
1266869171266869172TC34GENIChomozygous965888418
1266869354266869355CT32GENICpossibly homozygous965888419
1266871195266871196CT30GENIChomozygous965888420
1266871799266871800AG45GENIChomozygous965888421
1266872295266872296GA30GENIChomozygous965888422
1266876378266876379AG38GENIChomozygous965888423
1266876812266876813GA22GENIChomozygous965888424
1266878355266878356CT24GENICpossibly homozygous965888425
1266879795266879796TG25GENIChomozygous965888426
1266879804266879805AG26GENIChomozygous965888427
1266881234266881235CT42GENIChomozygous965888428
1266881721266881722AG28GENIChomozygous965888429
1266882385266882386GC32GENIChomozygous965888430
1266884148266884149CG15GENIChomozygous965888431
1266885292266885293AC28GENIChomozygous965888432
1266885604266885605GA30GENIChomozygous965888433
1266887077266887078GA17GENIChomozygous965888434
1266888529266888530CT18GENIChomozygous965888435
1266889651266889652TC18GENIChomozygous965888436
1266890046266890047TC33GENIChomozygous965888437
1266892447266892448AG16GENICpossibly homozygous965888438
1266892512266892513TC20GENIChomozygous965888439
1266894775266894776GA29GENIChomozygous965888440
1266895476266895477AG27GENIChomozygous965888441
1266896747266896748TG22GENICpossibly homozygous965888442
1266897388266897389TC41GENIChomozygous965888443
1266897506266897507GA22GENIChomozygous965888444
1266898357266898358AG23GENIChomozygous965888445
1266898962266898963GA21GENIChomozygous965888446
1266899513266899514GA27GENIChomozygous965888447
1266907705266907706AT25GENIChomozygous965888448