chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
18682902186829022TC25GENIChomozygous142844217
18682913886829139AG24GENIChomozygous142844218
18682947386829473TCTG36GENIChomozygous142790576
18683110086831101CT36GENIChomozygous145278233
18683231586832316AG35GENIChomozygous142844220
18683438986834390AT50GENIChomozygous142844224
18683571886835719CT44GENIChomozygous145278234
18683584586835846TA41GENICpossibly homozygous145278235
18683611086836111CA44GENIChomozygous145278236
18683887886838879AT50GENIChomozygous145278237
18683977986839780TA45GENIChomozygous145278238
18684062586840626AG37GENIChomozygous142844226
18684335986843360AG37GENIChomozygous142844235
18684905886849059GC37GENIChomozygous145278239
18684968286849683GA29GENIChomozygous142844260
18685107486851075AG45GENIChomozygous142844263
18685146186851462AC43GENIChomozygous142844264
18685146586851466AT42GENIChomozygous145278240
18685160086851601GA38GENIChomozygous145278241
18685212986852130TC37GENIChomozygous142844268
18685316386853164TC47GENIChomozygous145278242
18685334086853341AG37GENIChomozygous145278243
18685350186853502GC35GENIChomozygous145278244
18685354886853549GA44GENIChomozygous145278245
18685355486853555TC46GENIChomozygous142844270
18685392386853924CT43GENIChomozygous145278246
18685409086854091TA41GENIChomozygous145278247
18685409786854098AG41GENIChomozygous142844272
18685411986854120GA39GENIChomozygous145278248
18685418186854182TA33GENIChomozygous145278249
18685580886855809GA44GENIChomozygous145278250
18685587186855872CA49GENIChomozygous145278251
18684300186843002T42GENIChomozygous145235450
18684547586845475AAGA24GENIChomozygous145235451
18685180586851814GCCCACAGT35GENIChomozygous145235452