chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
155127822551278226T44GENICheterozygous129255599
155128172051281721GA19GENICheterozygous130701614
155128172651281727AC19GENICheterozygous130701615
155129010151290101A54GENIChomozygous129255602
155129391751293918AT55GENIChomozygous119024553
155129392651293927GT55GENIChomozygous118957520
155129393251293933AT54GENIChomozygous118918544
155129394651293947AT51GENIChomozygous118918545
155129395051293951TA51GENIChomozygous118918546
155129395351293954AT52GENIChomozygous118918547
155129389851293898CATCC49GENIChomozygous130440937
155129391951293919T56GENIChomozygous130440938
155129394251293942T51GENIChomozygous130440939
155129396151293961T50GENIChomozygous130440940
155129401451294015CA42GENIChomozygous113070656
155129407451294075AG35GENIChomozygous113070657
155129983451299835CG74GENICheterozygous129316724
155130093651300937C36GENIChomozygous129255606
155130963951309639T43GENIChomozygous129255611
155131245151312452GT20GENIChomozygous112507016
155131483551314836A9GENIChomozygous130149415
155131492151314925CACG43GENIChomozygous129255614
155131496951314970CA64GENIChomozygous112915483
155131503651315036G60GENIChomozygous129255615
155131508651315086C42GENIChomozygous129255616
155131512951315129T26GENIChomozygous129255617
155131513851315138C24GENIChomozygous129255618
155131515751315157T22GENIChomozygous129255619
155131517451315175G14GENIChomozygous129255620
155131518351315183C11GENIChomozygous129255621
155131547651315476T11GENIChomozygous129255622
155131547951315485GTGGCT11GENIChomozygous129255623
155131551151315512C26GENIChomozygous129255624
155131553451315535C34GENIChomozygous129255625
155134097351340974C66GENIChomozygous129255635
155134097651340977C67GENIChomozygous129255636
155136240751362407C41GENIChomozygous129255647
155129400251294003CA45GENIChomozygous113097390