chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3110669704110669705TC81GENIChomozygous112003935
3110669764110669765AG71GENIChomozygous112003937
3110671832110671833GA46GENIChomozygous112003939
3110671837110671838AG47GENIChomozygous112003941
3110672711110672712GC72GENIChomozygous112003943
3110673349110673350TA68GENIChomozygous111673167
3110673541110673542GA73GENIChomozygous112003945
3110674465110674466TC78GENIChomozygous111673170
3110674854110674855AG64GENICpossibly homozygous111673172
3110676064110676065GA47GENIChomozygous112003947
3110676197110676198GT41GENIChomozygous111673173
3110676200110676201TA39GENIChomozygous111673175
3110676206110676207GT41GENIChomozygous111673177
3110679217110679218CT46GENIChomozygous111673183
3110679539110679540GC76GENIChomozygous112003949
3110679818110679819CT57GENICpossibly homozygous112003951
3110680631110680632CA54GENIChomozygous112003953
3110682802110682803TC78GENICpossibly homozygous112003955
3110683140110683141TC73GENIChomozygous111673187
3110683392110683393GC42GENIChomozygous112003957
3110683410110683411CT50GENIChomozygous112003959
3110684387110684388AC69GENICpossibly homozygous111673190
3110689385110689386GC58GENICpossibly homozygous112003961
3110689389110689390AG59GENICpossibly homozygous111673194