chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2248737327248737328CT19GENIChomozygous110372474
2248739474248739475CT20GENIChomozygous110372476
2248740753248740754AG15GENIChomozygous110372478
2248741125248741126AG21GENIChomozygous110372480
2248742740248742741CG19GENIChomozygous110372482
2248743971248743972TC19GENIChomozygous110372484
2248744152248744153CT23GENIChomozygous110372486
2248745750248745751TC18GENIChomozygous110372490
2248747297248747298CT18GENIChomozygous110372491
2248749345248749346TC18GENIChomozygous110372495
2248753476248753477TC16GENIChomozygous110372497
2248755338248755339CA28GENIChomozygous110372499
2248765341248765342GT15GENIChomozygous110372501
2248738889248738899AGAAAGAGGC22GENIChomozygous127761210
2248768643248768644T14GENIChomozygous127761214
2248771089248771090CT18GENIChomozygous110372503
2248775944248775945GA17GENIChomozygous110372505
2248777397248777398CT23GENIChomozygous110372507
2248781961248781962GA16GENIChomozygous110372509
2248793771248793772AC28GENIChomozygous110372511
2248796625248796625A18GENIChomozygous127761215
2248797781248797782CA15GENIChomozygous110372513
2248799837248799838GA19GENIChomozygous110372515
2248806006248806007GA14GENICpossibly homozygous110372517
2248806020248806021AC14GENICpossibly homozygous110372519
2248806050248806050T16GENIChomozygous127761216
2248806053248806054T15GENICpossibly homozygous127761217
2248813755248813756GA23GENIChomozygous110372525
2248815685248815686TA25GENIChomozygous110372527
2248818866248818867CT19GENIChomozygous110372529
2248819653248819653T17GENIChomozygous127761218
2248820139248820140AG18GENIChomozygous110372531
2248821616248821617TC19GENIChomozygous110372533
2248831507248831508AG20GENIChomozygous110372535
2248835795248835796TC24GENIChomozygous110372537
2248837865248837865T12GENICheterozygous132568543
2248805400248805400T3GENIChomozygous129871304
2248811389248811389A19GENICheterozygous134082444