chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
57992278279922783CG28GENIChomozygous113888653
57992324679923247TC16GENIChomozygous114636279
57992342479923425GA8GENIChomozygous113888655
57992344379923444TC7GENIChomozygous118843675
57992344979923450AG6GENIChomozygous113888657
57992345679923457CT4GENIChomozygous113888659
57992387679923877TC14GENICpossibly homozygous113888661
57992459779924598AG16GENIChomozygous113888667
57992480579924806CT16GENIChomozygous113888673
57992519079925191TA17GENIChomozygous114636285
57992563779925638AG22GENIChomozygous113888681
57992581079925811CT27GENIChomozygous114636287
57992582479925825CT29GENIChomozygous114636289
57992754279927543CT34GENIChomozygous113888695
57992783679927837TC25GENIChomozygous113888697
57992908379929084TG11GENIChomozygous114636293
57992931979929320AC16GENIChomozygous113888699
57992933879929339AC16GENIChomozygous113888701
57993602879936029CT18GENIChomozygous113888707
57993656679936567AT14GENIChomozygous113888709
57994848179948482GA20GENIChomozygous114636301
57995315779953158AC41GENIChomozygous114636305
57995902779959028AG30GENIChomozygous113888745
57995934479959345AG30GENIChomozygous113888747
57995959179959592TC34GENIChomozygous114636307
57996020979960210CA19GENIChomozygous114636309
57996044579960446TG25GENIChomozygous113888753
57996607779966078AT25GENIChomozygous113888761