chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
14108491086108491087TC25GENIChomozygous113541344
14108492575108492576TC37GENIChomozygous113541346
14108494917108494918AC7GENIChomozygous118725429
14108495283108495284GC13GENIChomozygous118725430
14108496413108496414GA6GENIChomozygous114027029
14108497000108497001CG6GENIChomozygous118725431
14108497006108497007AG6GENIChomozygous118725432
14108498973108498974TC28GENIChomozygous113541348
14108500231108500232GA23GENIChomozygous113541350
14108500328108500329GC30GENIChomozygous113541352
14108500632108500633AG40GENIChomozygous113541354
14108501160108501161GT33GENIChomozygous113541356
14108501545108501546CA15GENICheterozygous118850200
14108504065108504066CG23GENIChomozygous113789757
14108505123108505124CT17GENIChomozygous113695060
14108505624108505625GA23GENIChomozygous113541364
14108502309108502310CA8GENIChomozygous113541358
14108502495108502496TA13GENIChomozygous113541360
14108502649108502650AG16GENIChomozygous113541362
14108505961108505962GA21GENIChomozygous113541366
14108507958108507959CT20GENIChomozygous113541368
14108509375108509376TG39GENIChomozygous113541370
14108510335108510336GA24GENIChomozygous113541372
14108511293108511294GA14GENIChomozygous113541374
14108511383108511384CA20GENICpossibly homozygous113789759
14108511532108511533AG13GENIChomozygous113541376
14108511866108511867GA16GENIChomozygous113541378
14108512264108512265CT13GENIChomozygous113541380
14108514018108514019AG37GENIChomozygous113541382
14108515726108515727GA14GENIChomozygous113541384
14108516013108516014TC24GENIChomozygous113541386
14108516799108516800TC34GENIChomozygous113541388
14108517480108517481GT23GENIChomozygous113541390