chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
17897762678977627TC20GENIChomozygous108873372
17897870878978709CT24GENIChomozygous109295344
17897927378979274CT21GENIChomozygous108873377
17897938978979390CT19GENIChomozygous108873379
17898330978983310AT27GENIChomozygous108873385
17898368578983686GA23GENIChomozygous120839290
17898381078983811TC34GENIChomozygous108873386
17898490378984904CT29GENICpossibly homozygous120839291
17898747278987473GA26GENIChomozygous120839292
17898771378987714TC12GENIChomozygous108873391
17898904178989042TG32GENIChomozygous108873394
17899010278990103AG19GENIChomozygous108873398
17899258778992588AG13GENIChomozygous108873406
17899300878993009TC20GENIChomozygous108873408
17899399578993996CA4GENIChomozygous120839293
17899567078995671AT26GENIChomozygous108873413
17899644878996449TG16GENIChomozygous108873415
17899645278996453TC16GENIChomozygous120839294
17899711378997114AG20GENIChomozygous120839295