chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
173349202133492022CG13GENIChomozygous111032134
173349202333492024AC14GENIChomozygous111032136
173349207633492077TA21GENIChomozygous111032138
173349207733492078AT21GENIChomozygous111032140
173350237133502372CA36GENIChomozygous111032144
173350237533502376GT36GENIChomozygous111032146
173356391933563920TC20GENIChomozygous111032152
173356399133563992CA14GENIChomozygous111032154
173356406733564068CA7GENIChomozygous111345837
173360125733601258TG2GENIChomozygous111193421
173360637233606373CT31GENICheterozygous111032162
173360655833606559TC55GENICheterozygous111193427
173360662933606630AG50GENICheterozygous111193428
173360665833606659TA45GENICheterozygous111032164
173360668433606685CA45GENICheterozygous111032166
173360689733606898CT45GENICheterozygous111032168
173360706933607070AG41GENICheterozygous111032170
173360808733608088TC41GENICheterozygous111032172
173360808833608089GA41GENICheterozygous111032174
173360817833608179AG64GENICheterozygous111032176
173360852133608522CT44GENICheterozygous111032178
173375948233759483GT18GENIChomozygous111193630
173375966433759665GT30GENIChomozygous111032190
173375996233759963AC27GENIChomozygous111032192
173376444733764448AC28GENIChomozygous111193657
173379269333792694CA31GENIChomozygous111032194
173380647633806477CT22GENIChomozygous111032196
173381035633810357GT22GENIChomozygous111032198
173384684233846843GA15GENIChomozygous111032204
173384688333846884GC24GENIChomozygous111032206
173387142633871427TC22GENIChomozygous111032214