chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
29605145396051454A31GENICheterozygous144273847
29605145396051454AG31GENIChomozygous153974811
29605367296053673TC44GENIChomozygous136225945
29605145496051455AG31GENIChomozygous136225943
29605189196051892GC49GENIChomozygous136225944
29605441496054415CT24GENIChomozygous136225946
29605473196054732AT35GENIChomozygous136225947
29605533496055335AG25GENIChomozygous136225948
29605564096055641CT41GENIChomozygous136225949
29605687296056873TA40GENIChomozygous136225950
29605755096057551GA52GENIChomozygous136225951
29605777396057774TC46GENIChomozygous136225952
29605857496058575AG47GENIChomozygous136225953
29605866696058667TG51GENIChomozygous136225954
29605925596059256AG33GENIChomozygous136225955
29606001496060015CG39GENIChomozygous136225956
29606034896060349CT31GENIChomozygous136225957
29606046996060470CG36GENIChomozygous136225958
29606058496060585CG37GENIChomozygous136225959
29606140996061410AG37GENIChomozygous136225960
29606306196063062GA58GENIChomozygous136225961
29606408396064084CT35GENIChomozygous136225962
29606512796065128CG39GENIChomozygous136225963
29606655396066554GA41GENIChomozygous136225964
29606686896066869TC44GENIChomozygous136225965
29606719196067192TG37GENIChomozygous136225966
29606823896068239AG29GENIChomozygous136225967
29606833996068340GT31GENIChomozygous136225968
29607004896070049CT38GENIChomozygous136225970
29607064896070649TC34GENIChomozygous136225971
29607070596070706GA40GENIChomozygous136225972
29607072596070726TC41GENIChomozygous136225973
29607108396071084TC37GENIChomozygous136225974
29607132596071326CT47GENIChomozygous136225975
29607188896071889T34GENICpossibly homozygous135929789
29605382496053825T33GENIChomozygous135929786
29606867196068671A33GENIChomozygous135929787
29607083396070833T42GENICpossibly homozygous135929788