chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
108148763881487639TA43GENIChomozygous525379860
108148766381487664AG36GENIChomozygous525379861
108148769881487699GA37GENIChomozygous525379862
108148869581488696GA50GENIChomozygous528148585
108148878581488791TCTATG------13GENIChomozygous692800989
108148923881489239GA29GENIChomozygous525379863
108148924281489243TC28GENIChomozygous525379864
108148934681489347TC29GENIChomozygous528148586
108148946981489470GA22GENIChomozygous525379865
108148956581489566GT41GENIChomozygous525379866
108148957181489572AT39GENIChomozygous525379867
108148993781489938GA23GENICheterozygous528148587
108148994881489949AAAAAAATAATATAT19GENICpossibly homozygous692800990
108149009181490092AG26GENIChomozygous525379868
108149035981490360CT43GENIChomozygous528148588
108149092581490926AT17GENIChomozygous525379869
108149102281491023GA36GENIChomozygous525379870
108149107981491080AC30GENIChomozygous525379871
108149111981491120GA36GENICpossibly homozygous525379872
108149135181491352AG32GENIChomozygous525379873
108149171281491713TTG39GENIChomozygous692800991
108149173681491737GT41GENIChomozygous525379874
108149177481491775AG41GENIChomozygous528148589
108149180481491805GA40GENIChomozygous528148590
108149215281492153CT30GENIChomozygous525379875
108149215881492159T-27GENIChomozygous692800992
108149256381492564GA38GENIChomozygous528148591
108149260381492604GA29GENIChomozygous528148592
108149320681493207AG21GENIChomozygous525379876
108149340981493410A-26GENIChomozygous692800993
108149346981493470TC35GENIChomozygous525379877
108149380981493810TC29GENIChomozygous528148593
108149407581494076TC39GENIChomozygous525379878
108149451081494511GA25GENIChomozygous528148594
108149506881495070AC--9GENIChomozygous692800995
108149566181495662AG21GENIChomozygous525379879
108149585781495858GA25GENIChomozygous528148595
108149604081496041CCT3GENICheterozygous692800996
108149643181496432TC30GENIChomozygous525379880