chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
139824709098247091G12GENIChomozygous129089291
139824719698247197C12GENIChomozygous129089292
139824720598247206G12GENIChomozygous129089293
139824721198247212GT12GENIChomozygous114583109
139824721398247214GT11GENIChomozygous114436306
139824723098247231G11GENIChomozygous129089294
139824722798247228AG11GENIChomozygous114436308
139824724498247245TC9GENIChomozygous114436310
139826530198265301C3GENIChomozygous129089308
139826530298265303AG3GENIChomozygous123790590
139826534698265346C8GENIChomozygous129089309
139826674798266748CT15GENIChomozygous114436366
139826674998266749ATG15GENIChomozygous129089310
139826693798266937G10GENIChomozygous129089311
139826801498268015TA7GENICheterozygous118505397
139826790898267909GT11GENICheterozygous130423596
139826791298267913TG11GENICheterozygous130423597
139826802198268022GA7GENICheterozygous118536939
139827441198274412GT17GENIChomozygous114583111
139827444398274444G20GENIChomozygous129089319
139826795498267963CCTCTGAAG12GENICheterozygous130419546
139827441498274414A17GENIChomozygous129089318
139827444798274451GACG20GENIChomozygous129089320
139827445498274455TG20GENIChomozygous114583113
139827445698274457CT20GENIChomozygous114583115
139827445898274459GT20GENIChomozygous114583117
139827446298274463G17GENIChomozygous129089321
139827447698274479GCG16GENIChomozygous129089322
139827448098274481GT15GENIChomozygous114583119
139827448298274483GT15GENIChomozygous114436376
139827448298274482A15GENIChomozygous129089323
139827462498274624A15GENIChomozygous129089324
139828141098281411GT11GENIChomozygous118529427
139828145898281459CG14GENIChomozygous118467071
139828931198289312TA16GENIChomozygous118505403
139828933398289334CT14GENIChomozygous118467072
139828979298289793TC2GENIChomozygous123839519
139829572298295723GT3GENIChomozygous118467073
139836178898361789T14GENICheterozygous131136034
139828977898289779G2GENIChomozygous133684152