chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
87569185075691851CT23GENIChomozygous116968368
87570220375702204GA30GENIChomozygous116968369
87570359375703594CT36GENIChomozygous116968370
87570396175703962AG35GENIChomozygous116968371
87570409075704091GC29GENIChomozygous116968372
87570429775704298CT21GENIChomozygous116968373
87570459575704596GA21GENIChomozygous116968374
87570572075705721AG29GENIChomozygous116968375
87570674075706741CA29GENIChomozygous116968376
87570697275706973AG26GENIChomozygous116968377
87570737675707377AC40GENIChomozygous116968378
87570843375708434GA38GENIChomozygous116968379
87570893075708931CT33GENIChomozygous116968380
87570899675708997CT32GENIChomozygous116968381
87570905675709076TGTGTGTATGTGTGTGTGTC26GENIChomozygous131049303
87570332675703327C32GENIChomozygous131049300
87570894875708950TG33GENIChomozygous131049301
87570902075709022TG28GENIChomozygous131049302
87571031475710315GA37GENIChomozygous116968382
87571214175712142AG29GENIChomozygous116968383
87571225275712253CT33GENIChomozygous116968384
87571315075713151TC16GENIChomozygous116968385
87571358975713590AG6GENIChomozygous116968386
87571422775714228AG16GENIChomozygous116968388
87571550575715505T25GENICpossibly homozygous131049304
87571591075715911AG41GENIChomozygous116968389
87571615175716152CT18GENIChomozygous116968390
87571672575716726TG26GENIChomozygous116968391
87571675175716752CG27GENIChomozygous116968392
87571705075717050C37GENIChomozygous131049305
87571823975718240CT38GENIChomozygous116968393
87571872875718729CT29GENIChomozygous116968394
87571967875719692TGTGTGTGTGTGTG25GENIChomozygous131049306
87572008375720084AG31GENIChomozygous116968395
87572036575720366AG35GENIChomozygous116968396
87572037175720372TC37GENIChomozygous116968397
87572148275721483TC32GENIChomozygous116968398
87572157075721571GA30GENIChomozygous116968399
87572162375721624CT31GENIChomozygous116968400
87572283675722837CT18GENIChomozygous116968402
87572286175722861TG20GENIChomozygous131049307
87572321575723216TC27GENIChomozygous116968403