chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1282142514282142515AT29GENIChomozygous108670827
1282144368282144369GA22GENIChomozygous108670828
1282144486282144487AC21GENIChomozygous108670829
1282144863282144864AG19GENIChomozygous108670830
1282145471282145472AT27GENIChomozygous108670831
1282148607282148608GA22GENIChomozygous108670832
1282150157282150158TA25GENIChomozygous109386859
1282150641282150642CT14GENIChomozygous108670833
1282151239282151240TC25GENIChomozygous108670834
1282152445282152446AG18GENICpossibly homozygous108670835
1282152616282152617TA29GENIChomozygous108670836
1282152971282152972TC31GENIChomozygous108670837
1282153710282153711TC20GENIChomozygous108670838
1282156377282156378AT26GENIChomozygous108670839
1282156443282156444TC27GENIChomozygous108670840
1282157370282157371AG23GENIChomozygous108670841
1282162332282162333CT28GENIChomozygous108670842
1282162800282162801GA36GENIChomozygous108670843
1282165523282165524CG25GENIChomozygous108670844
1282166029282166030CG17GENIChomozygous108670845
1282169541282169542CG22GENIChomozygous108670846