chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
549838404983841GA25GENIChomozygous114166448
549851144985115GA35GENIChomozygous113631014
549852204985221CG26GENIChomozygous113631015
549867724986773TC32GENIChomozygous113631016
549873484987349GA17GENIChomozygous113631017
549890904989091GA18GENIChomozygous114166450
549891594989160TC20GENIChomozygous113631019
549902794990280TC28GENIChomozygous113631021
549907124990713AT29GENIChomozygous113631023
549909814990982GA41GENICheterozygous114470590
549917254991726AG26GENIChomozygous114166452
549922274992228GA25GENIChomozygous113631026
549935834993584TA27GENIChomozygous113631029
549942464994247AG19GENIChomozygous113631030
549948814994882CT27GENICheterozygous113631031
549953014995302AC33GENIChomozygous113631032
549960034996004GC34GENIChomozygous113631033
549972894997290AG22GENIChomozygous113631034
549976844997685CT37GENIChomozygous113631035
549978574997858GA40GENIChomozygous113631036
549982664998267AG39GENIChomozygous113631037
549990304999031CT39GENIChomozygous113631038
550003605000361CT24GENIChomozygous113631039
550006355000636CT27GENIChomozygous113631040
550007845000785CG29GENIChomozygous113631041
550009575000958GC33GENIChomozygous113631042
550009605000961AT34GENIChomozygous113631043
550014725001473CT29GENIChomozygous114166458
550015265001527CT32GENIChomozygous113631044
550025795002580CT23GENIChomozygous113631045
550026895002690CT45GENICheterozygous113631046
550027175002718TC44GENICheterozygous113631047
550028665002867CT21GENIChomozygous114166460
550042215004222AG44GENIChomozygous113631048