chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
103653234936532350TC21GENIChomozygous138766681
103653297536532976TA20GENIChomozygous144866197
103653359936533600GT20GENIChomozygous138766683
103653391136533912CT18GENIChomozygous144866198
103653546336535464TC19GENIChomozygous138766684
103653567636535677TC16GENIChomozygous138766685
103653677236536773CA16GENIChomozygous144866199
103653680036536801TC16GENIChomozygous138766686
103653704636537047CT13GENIChomozygous144866200
103653353736533541CTGT18GENIChomozygous144855435
103653651936536519C11GENICpossibly homozygous144855436
103653718336537184CT18GENIChomozygous142232674
103653791636537917TC23GENIChomozygous138766689
103653967736539678CT13GENIChomozygous144866201
103654172436541725AG14GENIChomozygous138766697
103654338836543389CT17GENIChomozygous144866202
103654565836545659AT16GENIChomozygous144866203
103653432936534330AC25GENIChomozygous154628742
103653432936534330AT25GENICheterozygous154628743
103653449136534492CT11GENIChomozygous154628744
103655278336552783CCCTCTCC1GENIChomozygous144855438
103655532036555321CT23GENIChomozygous144866204
103655554736555548A6GENIChomozygous403282548
103655554736555548AG6GENICheterozygous403282549
103655554836555549A6GENIChomozygous403282550
103655554836555549AT6GENICheterozygous403282551
103655564436555645G20GENIChomozygous144855439