chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7121882953121882955AC--12GENICheterozygous55096574
7121883305121883309TGTG----10GENICheterozygous55096578
7121883615121883616TTG31GENIChomozygous54087330
7121892321121892322CCA42GENIChomozygous54087331
7121892323121892324TA40GENIChomozygous54921281
7121892332121892333G-42GENIChomozygous54087332
7121892362121892363CT36GENIChomozygous54087333
7121892388121892389G-27GENIChomozygous54087334
7121892402121892403T-23GENIChomozygous54087335
7121892413121892414G-20GENIChomozygous54087336
7121897703121897704GGA11GENICheterozygous54087337
7121897704121897705A-11GENICheterozygous55002607
7121904644121904645TTA17GENIChomozygous54087339
7121905908121905912GTGT----7GENICheterozygous55096582
7121905910121905912GT--7GENICheterozygous55096584
7121907447121907448G-11GENIChomozygous54087341
7121907451121907452GT12GENIChomozygous54921283
7121907464121907465T-9GENIChomozygous54087342
7121907471121907472CA9GENIChomozygous54087343
7121907472121907473AC9GENIChomozygous54087344
7121908843121908844CA30GENIChomozygous54087345
7121909706121909707CT25GENIChomozygous54087346