chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
29605145396051454A14GENICheterozygous144273847
29605145396051454AG14GENICpossibly homozygous153974811
29605145496051455AG14GENIChomozygous136225943
29605189196051892GC22GENIChomozygous136225944
29605367296053673TC25GENIChomozygous136225945
29605441496054415CT28GENIChomozygous136225946
29605473196054732AT19GENIChomozygous136225947
29605533496055335AG21GENIChomozygous136225948
29605564096055641CT13GENIChomozygous136225949
29605687296056873TA20GENIChomozygous136225950
29605755096057551GA20GENIChomozygous136225951
29605777396057774TC34GENIChomozygous136225952
29605857496058575AG20GENIChomozygous136225953
29605866696058667TG22GENIChomozygous136225954
29605925596059256AG18GENIChomozygous136225955
29606001496060015CG12GENIChomozygous136225956
29606034896060349CT18GENIChomozygous136225957
29606046996060470CG16GENIChomozygous136225958
29606058496060585CG20GENIChomozygous136225959
29606140996061410AG15GENIChomozygous136225960
29606306196063062GA15GENIChomozygous136225961
29606408396064084CT20GENIChomozygous136225962
29606512796065128CG19GENIChomozygous136225963
29606655396066554GA19GENIChomozygous136225964
29606686896066869TC31GENIChomozygous136225965
29607070596070706GA15GENIChomozygous136225972
29605382496053825T18GENIChomozygous135929786
29606867196068671A20GENIChomozygous135929787
29606719196067192TG28GENIChomozygous136225966
29606823896068239AG36GENIChomozygous136225967
29606833996068340GT25GENIChomozygous136225968
29607004896070049CT14GENIChomozygous136225970
29607064896070649TC14GENIChomozygous136225971
29606069496060695TC23GENIChomozygous149208029
29607072596070726TC16GENIChomozygous136225973
29607083396070833T22GENIChomozygous135929788
29607108396071084TC22GENIChomozygous136225974
29607132596071326CT16GENIChomozygous136225975
29607188896071889T14GENIChomozygous135929789