chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5141009739141009740TC4GENIChomozygous114031324
5141009874141009875GT6GENIChomozygous114031325
5141010775141010776AG9GENIChomozygous114031327
5141010900141010901AG13GENIChomozygous114031328
5141011168141011169AG10GENIChomozygous114031329
5141012461141012462TC7GENIChomozygous114031331
5141012981141012982GA8GENIChomozygous114031332
5141013782141013783CA5GENIChomozygous114031334
5141014103141014104AT3GENIChomozygous119258190
5141015028141015029CT11GENICheterozygous114031338
5141015245141015246AT10GENICheterozygous114031339
5141015385141015386GA10GENICheterozygous114031340
5141015400141015401CT9GENICpossibly homozygous114031341
5141015417141015418TC9GENIChomozygous114031342
5141015689141015690TC7GENICpossibly homozygous114031345
5141015908141015909CT9GENIChomozygous114031347
5141015912141015913AG9GENIChomozygous114031348
5141015950141015951GC12GENIChomozygous114031350
5141016016141016017CA4GENIChomozygous114031353
5141020090141020091AG5GENIChomozygous114031363
5141020893141020894AT3GENIChomozygous114031365
5141021304141021305TA6GENIChomozygous119182743
5141020978141020979TA5GENIChomozygous119182741
5141021281141021282GT5GENIChomozygous119182742
5141022623141022624TC8GENIChomozygous114031370
5141022708141022709GA10GENIChomozygous119182744
5141024499141024500AG9GENIChomozygous114031373
5141025148141025149CT4GENIChomozygous119182745
5141027851141027852CT6GENIChomozygous119182746
5141030627141030628GT3GENIChomozygous114031380
5141030711141030712TC7GENIChomozygous114031381
5141031083141031084TC11GENIChomozygous114031382
5141031147141031148GC11GENIChomozygous119182748
5141031657141031658AG5GENIChomozygous114031384