chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8111982463111982464TC12GENICheterozygous52815146
8111982560111982561AG13GENICheterozygous53036077
8111991629111991630AG34GENICheterozygous53036296
8111993746111993747AG11GENICheterozygous53036368
8112007706112007707GA35GENICheterozygous53036394
8112007711112007712CA35GENICheterozygous53036396
8112007875112007876TC17GENICheterozygous53036400
8112007907112007908AG10GENICheterozygous53410009
8112007908112007909TA10GENICheterozygous53410011
8112007919112007920CT9GENICheterozygous52815172
8112009973112009974TC33GENICheterozygous53036456
8112013873112013874TC13GENICheterozygous53036504
8112027005112027006AG19GENICheterozygous53036636
8112027014112027015CT19GENICheterozygous53036638
8112028754112028755CT17GENICheterozygous53036662
8112028807112028808GA18GENICheterozygous53036664
8112028814112028815CT18GENICheterozygous53036666
8112028858112028860TG--16GENICheterozygous53036668
8112031561112031562AG19GENICheterozygous52815304
8112032102112032103CG27GENICheterozygous53036727
8112032141112032142AG24GENICheterozygous52815309
8112034510112034511AAGATCT9GENICheterozygous53410059
8112034512112034516GAAA----7GENICheterozygous53410061
8112035362112035363GGT16GENICheterozygous53036771
8112035372112035373AG17GENICheterozygous53036773
8112035471112035472CA9GENICheterozygous53036775
8112061739112061740TC27GENICheterozygous53037178
8112061805112061806CT41GENICheterozygous53037180
8112061963112061964CT36GENICheterozygous53037182
8112061968112061969GA35GENICheterozygous53037184
8112062282112062283GA24GENICheterozygous53037186
8112062330112062331AG21GENICheterozygous53037188
8112062419112062420TC33GENICheterozygous53037190
8112062443112062444AG38GENICheterozygous53037192