chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141388994141388995TC12GENIChomozygous56065373
5141389000141389001GA9GENIChomozygous56065374
5141389003141389004CT8GENIChomozygous56065375
5141389024141389025TC8GENIChomozygous56065376
5141389030141389031AG9GENIChomozygous56065377
5141389033141389034CG9GENIChomozygous56065378
5141389080141389081TG16GENIChomozygous56065379
5141389325141389326GA19GENICpossibly homozygous56065380
5141389605141389606CT28GENICpossibly homozygous56065381
5141389717141389718AC17GENIChomozygous56065382
5141389803141389804TG23GENICheterozygous56065383
5141389843141389844AG17GENICheterozygous56065384
5141389867141389868AG23GENICpossibly homozygous56065385
5141389872141389873CG23GENIChomozygous56065386