chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
76537929865379299T-14GENICheterozygous53943373
76539708865397089CCT23GENICheterozygous53943374
76540766565407666CG37GENIChomozygous53943375
76540774465407745CT41GENIChomozygous53943376
76540777765407778TTG37GENIChomozygous53943377
76540922965409230GGCATAT17GENICpossibly homozygous53943378
76540930865409310AC--13GENICheterozygous53943379
76541657265416573TTGACAAG27GENIChomozygous53943380
76542168165421682TG32GENICheterozygous53943381
76542307765423078TTTTAG40GENIChomozygous53943382
76542349965423500CCA14GENICheterozygous53943383
76544141665441417TG29GENICheterozygous53943384
76544316065443161CCT12GENICheterozygous53943385
76544490965444910TC41GENICheterozygous53943386
76545844665458447T-34GENICheterozygous53943387
76545845965458460A-17GENICheterozygous53943388
76546408365464085CA--13GENICheterozygous53943389
76547434165474342TC18GENICpossibly homozygous53943390
76547434365474344TC18GENICpossibly homozygous53943391
76547434865474349GT16GENIChomozygous53943392
76547435165474352TC19GENICheterozygous53943393
76547436165474362GC15GENIChomozygous53943394
76547436365474364GC15GENIChomozygous53943395
76547442265474423TG11GENIChomozygous53943396
76547443765474438AT13GENIChomozygous53943397
76547444165474442TC12GENIChomozygous53943398
76547445365474454TG17GENIChomozygous53943399
76547445765474458AC16GENIChomozygous53943400
76547445965474460TC18GENIChomozygous53943401
76547446165474462GC19GENIChomozygous53943402
76547483865474839T-39GENIChomozygous53943403
76547780865477809GGGA17GENICheterozygous53943404
76547780865477809GGGAGGGAGAGAGA17GENICheterozygous53943405
76547825065478251G-42GENIChomozygous53943406
76547849965478500TG5GENIChomozygous53943407
76548206865482069A-10GENIChomozygous53943408
76548497565484976A-24GENICheterozygous53943409
76548497565484976AAG25GENIChomozygous53943410
76548788465487885A-1GENIChomozygous53943411