chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105958510559585106GA60GENIChomozygous51663669
105958926759589268C-44GENIChomozygous51663671
105958950159589502CA61GENICpossibly homozygous51663673
105958976759589768TC73GENIChomozygous51465835
105959050559590506GA57GENIChomozygous51663675
105959058559590586GA48GENIChomozygous51663677
105959129359591300GGCATTT-------21GENIChomozygous51465836
105959157059591571GA36GENIChomozygous51663679
105959166459591672TGTGTGTG--------4GENIChomozygous51663681
105959289659592897CA47GENIChomozygous51663683
105959307559593076CA80GENIChomozygous51663685
105959390759593908TC53GENIChomozygous51465837
105959579159595792CT65GENIChomozygous51663687
105959605159596052GA80GENIChomozygous51663689
105959659559596596TTAA41GENIChomozygous51663691
105959680659596807GA53GENIChomozygous51663693
105959695859596959TC69GENIChomozygous51663695
105959701859597019TA64GENIChomozygous51663697
105959710459597105AAG37GENIChomozygous51663699
105959710559597106GGC25GENICheterozygous51465838
105959710559597106GGGC25GENICheterozygous51663701
105959741759597418CT51GENICpossibly homozygous51663703
105959826159598262TTATC49GENIChomozygous51663705
105959887359598874AT70GENIChomozygous51663707
105959928459599285GT55GENIChomozygous51465839
105959948459599485CT52GENIChomozygous51663709
105959989959599900GA43GENIChomozygous51663711
105960012859600129G-45GENIChomozygous51465841
105960068259600683GGTTT30GENICpossibly homozygous51465842
105960068259600683GGTT30GENICheterozygous51465843
105960255859602559AG100GENIChomozygous51663713
105960478259604783CA57GENICpossibly homozygous51663715
105960485859604859AAGTGT16GENICheterozygous51465845
105960489859604899CT41GENICpossibly homozygous51663717
105960625859606259CT60GENIChomozygous51663719
105960633659606337AG48GENIChomozygous51663721
105960650559606506CT64GENIChomozygous51465846
105960771959607726TTTTTTT-------13GENIChomozygous51663723
105960774459607745TC32GENICheterozygous51663725