chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
11769257017692571TC51GENIChomozygous141195106
11787123617871236AC15GENICheterozygous149269328
11808322918083230TC50GENICpossibly homozygous135508256
11809376618093767AT32GENICheterozygous140852302
11812188618121887AG43GENIChomozygous141195109
11814648018146483GAG30GENICheterozygous149269329
11793158117931582T53GENICpossibly homozygous135396905
11797197917971980CT23GENICheterozygous402941245
11797197917971980C23GENIChomozygous402941246
11803361118033612A7GENICheterozygous402941247
11803361118033612AG7GENICheterozygous402941248
11809377618093777CT31GENICheterozygous402941249
11815923518159237GT46GENICheterozygous140957141
11819008118190082G20GENICheterozygous140957142
11820665218206656TCTG6GENIChomozygous135396907
11824825118248252A53GENICheterozygous141110789
11827743318277434GT29GENIChomozygous135508259
11827745018277451GC33GENIChomozygous135508260
11830603418306035GC42GENIChomozygous141195110