chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
99073346490733465GGT17GENIChomozygous691049404
99073349690733497GGT14GENIChomozygous691049405
99073383290733834GT--5GENICheterozygous691049407
99073603090736031TTGGGA26GENIChomozygous691049408
99073687890736879TG22GENIChomozygous520789094
99073692190736922TG27GENIChomozygous520789095
99073693290736933TG27GENIChomozygous520789096
99073694690736947AG25GENIChomozygous520789097
99073695490736955TG24GENIChomozygous520789098
99073697190736972TA24GENIChomozygous520789099
99073838490738385CT26GENICheterozygous521991380
99073856290738563TC32GENICpossibly homozygous521991381
99073860890738609GA23GENICpossibly homozygous521991382
99073864990738650CT29GENICpossibly homozygous521991383
99073977590739776TC27GENICheterozygous521991384
99073982890739830AA--23GENIChomozygous691049409
99073995190739952AT33GENICheterozygous521991385
99073996690739967TC29GENICheterozygous521991386
99074061090740612AT--1GENIChomozygous691049410
99074067290740673CT22GENICheterozygous521991387
99074145590741456AAAGG10GENIChomozygous691049411
99074148190741482TA14GENIChomozygous521991388
99074148690741487GA13GENIChomozygous521991389
99074230990742310TC22GENICheterozygous521991390
99074242690742428AA--25GENIChomozygous691049412
99074244890742449GT22GENIChomozygous521991391
99074245490742455TG23GENICpossibly homozygous521991392
99074253790742538CT12GENICheterozygous521991393
99074258390742584CT8GENICheterozygous521991394
99074258590742586TC8GENICheterozygous521991395
99074769090747691T-31GENICheterozygous691049413
99074769090747691TTAG35GENICpossibly homozygous691049414
99074769290747693A-34GENICheterozygous691049415
99074780190747802CG53GENICheterozygous521991396
99074795090747951CT40GENIChomozygous521991397
99074795390747954CA38GENICpossibly homozygous521991398
99074796890747969CT41GENIChomozygous521991399
99074797490747975CT40GENIChomozygous521991400
99074803190748032CT51GENIChomozygous521991401
99074958090749581G-34GENICheterozygous691049416