chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14108491086108491087TC30GENIChomozygous113541344
14108492575108492576TC20GENIChomozygous113541346
14108498973108498974TC17GENIChomozygous113541348
14108500231108500232GA25GENIChomozygous113541350
14108500328108500329GC18GENIChomozygous113541352
14108500632108500633AG23GENIChomozygous113541354
14108501160108501161GT16GENIChomozygous113541356
14108502309108502310CA19GENIChomozygous113541358
14108502495108502496TA22GENIChomozygous113541360
14108502649108502650AG10GENIChomozygous113541362
14108505624108505625GA31GENIChomozygous113541364
14108505961108505962GA24GENIChomozygous113541366
14108506971108506972AG2GENIChomozygous113618392
14108507958108507959CT27GENIChomozygous113541368
14108509375108509376TG32GENIChomozygous113541370
14108510335108510336GA20GENIChomozygous113541372
14108511293108511294GA17GENIChomozygous113541374
14108511532108511533AG18GENIChomozygous113541376
14108511866108511867GA16GENIChomozygous113541378
14108512264108512265CT18GENIChomozygous113541380
14108514018108514019AG17GENIChomozygous113541382
14108515726108515727GA27GENIChomozygous113541384
14108516013108516014TC29GENIChomozygous113541386
14108502524108502525A17GENIChomozygous129193976
14108495309108495310C13GENIChomozygous130142343
14108501553108501553AC14GENIChomozygous129193974
14108501566108501566CA16GENIChomozygous129193975
14108506965108506965GGGA3GENIChomozygous129193977
14108509489108509490A24GENIChomozygous129193978
14108514363108514364G20GENICpossibly homozygous129193979
14108501557108501558CA15GENIChomozygous113789755
14108504065108504066CG26GENIChomozygous113789757
14108511383108511384CA10GENIChomozygous113789759
14108505123108505124CT32GENIChomozygous113695060
14108513805108513806AT14GENIChomozygous113765908
14108516799108516800TC20GENIChomozygous113541388
14108517480108517481GT21GENIChomozygous113541390