chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8121235409121235413TGGA----8GENIChomozygous53412854
8121236706121236708GG--18GENIChomozygous52853883
8121236711121236718CCAGAGT-------18GENIChomozygous52853885
8121236723121236724TC23GENIChomozygous52853889
8121236726121236727TA26GENIChomozygous53368462
8121236727121236728GT27GENIChomozygous53368463
8121236745121236746AC30GENIChomozygous52853891
8121236759121236760CA29GENIChomozygous53368464
8121236760121236761GC28GENIChomozygous53368465
8121236772121236773AT28GENIChomozygous52853893
8121236788121236789GT33GENIChomozygous52853895
8121236791121236792A-32GENIChomozygous52853897
8121236799121236800AAG30GENIChomozygous52853899
8121236815121236816CA27GENIChomozygous52853901
8121236821121236822T-27GENIChomozygous52853903
8121236838121236839A-32GENIChomozygous52853905
8121236849121236850GT34GENIChomozygous52853907
8121236853121236854G-33GENIChomozygous52853909
8121236885121236886T-35GENIChomozygous52853911
8121236895121236896G-39GENIChomozygous52853913
8121236899121236900C-39GENIChomozygous52853915
8121236914121236915T-40GENIChomozygous52853917
8121240756121240757A-38GENIChomozygous52853919
8121250222121250223A-4GENICheterozygous53168805
8121251429121251431CC--16GENICheterozygous53474300
8121251430121251431C-16GENICheterozygous53412855
8121255565121255566AC22GENICpossibly homozygous52853921
8121257642121257643CCTG2GENIChomozygous53412856
8121262134121262135A-8GENICheterozygous52853929
8121263698121263699CCA6GENICheterozygous53412858
8121270797121270798G-26GENIChomozygous52853933
8121270936121270938AC--14GENIChomozygous52853935
8121285844121285845AAC16GENICheterozygous53412860