chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111982463111982464TC25GENICheterozygous52815146
8111982560111982561AG6GENICheterozygous53036077
8111991629111991630AG42GENICheterozygous53036296
8111993746111993747AG25GENICheterozygous53036368
8112007706112007707GA27GENICheterozygous53036394
8112007711112007712CA27GENICheterozygous53036396
8112007875112007876TC17GENICheterozygous53036400
8112007907112007908AG14GENICheterozygous53410009
8112007908112007909TA14GENICheterozygous53410011
8112007919112007920CT13GENICheterozygous52815172
8112009973112009974TC39GENICheterozygous53036456
8112013873112013874TC30GENICheterozygous53036504
8112027005112027006AG22GENICheterozygous53036636
8112027014112027015CT19GENICheterozygous53036638
8112028754112028755CT19GENICheterozygous53036662
8112028807112028808GA17GENICheterozygous53036664
8112028814112028815CT18GENICheterozygous53036666
8112028858112028860TG--21GENICheterozygous53036668
8112031561112031562AG23GENICheterozygous52815304
8112032102112032103CG30GENICheterozygous53036727
8112032141112032142AG20GENICheterozygous52815309
8112035362112035363GGT12GENICheterozygous53036771
8112035372112035373AG17GENICheterozygous53036773
8112035471112035472CA23GENICheterozygous53036775
8112046289112046290CT13GENICheterozygous53037003
8112046293112046294GGC13GENICheterozygous53037005
8112061739112061740TC54GENICheterozygous53037178
8112061805112061806CT43GENICheterozygous53037180
8112061963112061964CT34GENICheterozygous53037182
8112061968112061969GA36GENICheterozygous53037184
8112062282112062283GA22GENICheterozygous53037186
8112062330112062331AG16GENICheterozygous53037188
8112062419112062420TC42GENICheterozygous53037190
8112062443112062444AG53GENICheterozygous53037192