chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135974862135974863GA41GENIChomozygous143962431
5135975191135975192CT31GENIChomozygous143962432
5135975209135975210TG30GENIChomozygous143962433
5135975556135975557TG37GENIChomozygous143962434
5135976235135976236GA38GENIChomozygous143962435
5135976288135976289GC43GENIChomozygous143962436
5135976614135976615AG51GENIChomozygous143962437
5135977092135977093GA49GENIChomozygous143962438
5135977093135977094AC50GENIChomozygous143962439
5135977303135977304TC39GENIChomozygous143962440
5135977444135977444A38GENIChomozygous143944524
5135977743135977744CT24GENIChomozygous143962441
5135977890135977891CT19GENIChomozygous143962442
5135977965135977966AC13GENIChomozygous143962443
5135978317135978318AG27GENICpossibly homozygous143962444
5135978660135978661TA38GENICpossibly homozygous143962445
5135977983135977984A11GENIChomozygous147262560