chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4142357946142357947CG11GENICheterozygous56960453
4142357972142357973TC17GENICheterozygous56960454
4142358001142358002GA15GENICheterozygous57342182
4142358124142358125AC10GENICheterozygous56960455
4142358706142358707GT19GENIChomozygous56960456
4142358714142358715TTA18GENIChomozygous56960457
4142362615142362616CT30GENIChomozygous57504463
4142364123142364124CCT13GENICpossibly homozygous56960460
4142365937142365938AG16GENICheterozygous56960462
4142372020142372021TC16GENIChomozygous56960465
4142372133142372134C-3GENIChomozygous56960466
4142372161142372162A-4GENIChomozygous56960467
4142372161142372162AAC4GENIChomozygous56960468
4142374612142374613GA24GENICheterozygous56960469
4142374612142374613GGTA20GENIChomozygous56960470
4142375043142375044GA26GENICpossibly homozygous56960472
4142377826142377827TC29GENIChomozygous56960473
4142378211142378212GT35GENIChomozygous57504466
4142378895142378896GGA22GENIChomozygous57504468