chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4169164736169164737TC18GENIChomozygous112946340
4169164843169164844CT20GENIChomozygous112946342
4169164886169164887TA23GENIChomozygous112946344
4169164905169164906TC26GENIChomozygous112946346
4169164910169164911TG28GENIChomozygous112946348
4169164960169164961TC30GENIChomozygous112946350
4169165133169165134GC26GENIChomozygous112946352
4169165139169165140GT27GENIChomozygous112946354
4169165141169165142AG26GENIChomozygous112946356
4169165264169165265TC23GENIChomozygous112946358
4169165293169165294TC22GENIChomozygous112946360
4169165479169165480GA25GENIChomozygous112946362
4169165913169165914TC18GENIChomozygous112946364
4169165990169165991AG23GENIChomozygous112946366
4169166156169166157CT21GENIChomozygous112946368
4169166159169166160AT21GENIChomozygous112946370
4169166294169166295TA21GENIChomozygous112946372
4169166592169166593CA20GENIChomozygous112946374
4169166786169166787TC28GENIChomozygous112946376
4169166973169166974AG10GENIChomozygous112946378
4169167294169167295AC13GENIChomozygous112946380
4169168564169168565AT13GENIChomozygous112946386
4169168891169168892TC15GENIChomozygous112946388
4169169291169169292TC22GENIChomozygous112946390
4169180592169180593TC18GENIChomozygous113476761