chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14108491086108491087TC59GENIChomozygous113541344
14108492575108492576TC68GENIChomozygous113541346
14108496368108496384AGGAAGGAAGGAAGGA8GENIChomozygous131147512
14108498973108498974TC51GENIChomozygous113541348
14108500231108500232GA69GENIChomozygous113541350
14108500328108500329GC64GENIChomozygous113541352
14108500632108500633AG51GENIChomozygous113541354
14108501160108501161GT55GENIChomozygous113541356
14108502309108502310CA68GENIChomozygous113541358
14108502495108502496TA54GENIChomozygous113541360
14108502649108502650AG62GENIChomozygous113541362
14108505624108505625GA62GENIChomozygous113541364
14108505961108505962GA70GENIChomozygous113541366
14108506971108506972AG4GENIChomozygous113618392
14108507958108507959CT74GENIChomozygous113541368
14108509375108509376TG70GENIChomozygous113541370
14108510335108510336GA69GENIChomozygous113541372
14108511293108511294GA46GENIChomozygous113541374
14108511532108511533AG45GENIChomozygous113541376
14108511866108511867GA56GENIChomozygous113541378
14108512264108512265CT70GENIChomozygous113541380
14108514018108514019AG45GENIChomozygous113541382
14108515726108515727GA59GENIChomozygous113541384
14108516013108516014TC76GENIChomozygous113541386
14108516799108516800TC52GENIChomozygous113541388
14108517480108517481GT37GENIChomozygous113541390
14108513805108513806AT37GENIChomozygous113765908
14108495309108495310C27GENIChomozygous130142343
14108496413108496414GA6GENIChomozygous114027029
14108501553108501553AC23GENICpossibly homozygous129193974
14108501566108501566CA32GENIChomozygous129193975
14108502524108502525A63GENIChomozygous129193976
14108506965108506965GGGA7GENIChomozygous129193977
14108509489108509490A42GENIChomozygous129193978
14108514363108514364G61GENIChomozygous129193979
14108501557108501558CA27GENIChomozygous113789755
14108504065108504066CG39GENIChomozygous113789757
14108511383108511384CA27GENIChomozygous113789759
14108505123108505124CT67GENIChomozygous113695060