chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135048195950481960TG14GENIChomozygous114549954
135048221850482219GA24GENICpossibly homozygous114340522
135048308650483087TC28GENIChomozygous114671388
135048342350483424CT14GENIChomozygous114671390
135048411450484115TC32GENIChomozygous114340526
135048507450485075TC21GENIChomozygous114671392
135048530150485302GA21GENIChomozygous114671394
135048530350485304TG29GENIChomozygous114720336
135048551350485514TC20GENIChomozygous114671396
135048572350485724TG21GENIChomozygous114671398
135048587050485871GA21GENIChomozygous114671400
135048590250485903CT18GENIChomozygous114671402
135048592050485921TA24GENIChomozygous114671404
135048658650486587AG12GENIChomozygous114671406
135048665650486657AG14GENIChomozygous114340528
135048777050487771CT11GENIChomozygous114890156
135048834550488346TC22GENIChomozygous114340530
135048850250488503CT19GENIChomozygous114340532
135048906550489066GA27GENIChomozygous114340536
135048915750489158GA26GENIChomozygous114890158
135048918250489183AG19GENIChomozygous114340538
135048942650489427TG29GENIChomozygous114340540
135049027950490280TC22GENIChomozygous114340542
135049076150490762GA22GENIChomozygous114340544
135049141050491411GA19GENIChomozygous114890160
135049161150491612CA18GENIChomozygous114340546
135049180650491807TC25GENIChomozygous114340550
135049180850491809AG27GENIChomozygous114340552
135049204650492047GA24GENIChomozygous114340556
135049218750492188TC29GENIChomozygous114340558
135049262850492629TC20GENIChomozygous114340560
135049310450493105GA32GENIChomozygous114340566
135049326950493270CT24GENIChomozygous114340568
135049420250494203GC23GENIChomozygous114671418
135049605250496053GA28GENICpossibly homozygous114340578
135049862150498622TG18GENIChomozygous114340580