chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
102784918527849186AG51GENIChomozygous116750489
102785471727854718AG27GENIChomozygous116534383
102785502027855021GA12GENIChomozygous116534385
102785703227857033GT20GENIChomozygous116534387
102785762127857622CA7GENIChomozygous117177787
102785889827858899TC19GENIChomozygous116534393
102785895727858958CT22GENIChomozygous116534395
102785906727859068CT27GENIChomozygous116534397
102785909927859100CT30GENIChomozygous116534399
102785935427859355TC32GENIChomozygous116534401
102785967827859679TC17GENIChomozygous116534403
102785978627859787AC35GENIChomozygous116534405
102785981027859811AC45GENIChomozygous116534407
102786002827860029CT18GENIChomozygous116534409
102786012827860129GA11GENIChomozygous116534411
102786016627860167AT8GENIChomozygous116534413
102786059627860597TC25GENICpossibly homozygous116750491
102786065127860652AC24GENIChomozygous116534415
102786113327861134GA49GENIChomozygous116534417
102786152827861529AC43GENIChomozygous116534419
102786178227861783AG16GENIChomozygous117001239
102786179227861793TC12GENIChomozygous116750493
102786180827861809TC20GENIChomozygous117168845
102786251227862513AG33GENIChomozygous116534421
102786263027862631CA41GENIChomozygous116534423
102786272027862721AG25GENIChomozygous116534425