chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1101368760101368761AT33GENIChomozygous945816485
1101369073101369074AG36GENICpossibly homozygous945816486
1101370673101370674TC38GENIChomozygous945816487
1101370736101370737AT27GENIChomozygous945816488
1101370770101370771CT23GENIChomozygous945816489
1101371580101371581GC31GENIChomozygous945816490
1101372581101372582TC21GENIChomozygous945816491
1101376215101376216AG16GENIChomozygous945816492
1101376401101376402TG16GENIChomozygous945816493
1101380569101380570AG14GENIChomozygous945816494
1101380582101380583CT14GENIChomozygous945816495
1101380673101380674GA13GENIChomozygous945816496
1101381127101381128AG14GENIChomozygous945816497
1101382022101382023TG28GENIChomozygous945816498
1101383176101383177GA20GENIChomozygous945816499
1101383339101383340TC26GENIChomozygous945816500
1101384591101384592AG34GENIChomozygous945816501
1101385268101385269TC25GENIChomozygous945816502
1101385945101385946CA35GENIChomozygous945816503
1101387193101387194CT17GENIChomozygous945816504