chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
141728380217283803TG19GENIChomozygous991859397
141728481617284817CT11GENIChomozygous991859398
141728489917284900CT23GENIChomozygous991859399
141728505217285053TA6GENIChomozygous991859400
141728505817285059CT6GENIChomozygous991859401
141728520317285204GC12GENIChomozygous991859402
141728563217285633CT11GENIChomozygous991859403
141728587617285877CG17GENIChomozygous991859404
141728588117285882CT17GENIChomozygous991859405
141728604017286041GA16GENIChomozygous991859406
141728645617286457TC15GENIChomozygous991859407
141728669517286696CT14GENIChomozygous991859408
141728676817286769TA19GENIChomozygous991859409
141728677617286777TC21GENIChomozygous991859410
141728685817286859TC11GENIChomozygous991859411
141728703617287037CA8GENIChomozygous991859412
141728710317287104CT8GENIChomozygous991859413
141728766817287669TA15GENIChomozygous991859414
141729113417291135GA13GENIChomozygous991859415
141729148217291483GC15GENIChomozygous991859416
141729201917292020CT13GENIChomozygous991859417
141729228617292287GC16GENIChomozygous991859418
141729295017292951CT22GENIChomozygous991859419
141729299117292992TC23GENIChomozygous991859420
141729314017293141GA22GENIChomozygous991859421
141729327917293280AC22GENIChomozygous991859422
141729329117293292TC19GENIChomozygous991859423
141729348817293489AG16GENIChomozygous991859424
141729472117294722AG23GENIChomozygous991859425
141729490717294908AG25GENIChomozygous991859426
141729502417295025TC25GENIChomozygous991859427
141729540917295410CT20GENIChomozygous991859428
141729553717295538TC10GENIChomozygous991859429
141729591217295913TC15GENIChomozygous991859430
141729593717295938AG17GENIChomozygous991859431
141729638517296386AG19GENIChomozygous991859432
141730108917301090TG28GENIChomozygous991859433
141730127317301274TC27GENIChomozygous991859434