chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
144396354043963541GA25GENIChomozygous113443892
144396426843964269AG23GENIChomozygous113443894
144396443343964434AT27GENIChomozygous113443896
144396489343964894AC22GENICpossibly homozygous113443898
144396536543965366AC17GENIChomozygous113592935
144396872443968725TC17GENIChomozygous113592937
144396887943968880CG16GENIChomozygous113443900
144396919043969191TC28GENIChomozygous113443902
144397168443971685CT23GENIChomozygous113443904
144397235943972360TG20GENIChomozygous113443906
144397321143973212CG19GENIChomozygous113443908
144397529343975294GA22GENIChomozygous113443912
144397530843975309GT22GENIChomozygous113443914
144397561843975619CT28GENIChomozygous113443916
144398037543980376AG31GENIChomozygous113443918
144398061443980615GC30GENIChomozygous113443920
144398182943981830TA25GENIChomozygous113443922
144398343343983434CT41GENIChomozygous113443924
144398437443984375CT30GENIChomozygous113443926
144398486743984868CT13GENIChomozygous113443928
144398757543987576CT26GENIChomozygous113443930
144398765343987654AG27GENIChomozygous113443932
144399195143991952AG29GENIChomozygous113443934
144399217143992172TC27GENIChomozygous113443936