chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3130622937130622938TTGGG2GENIChomozygous57675484
3130624447130624448AG16GENICpossibly homozygous57675489
3130625837130625838GA26GENIChomozygous57675491
3130628078130628079GA13GENICheterozygous57675493
3130628320130628321GA3GENICheterozygous57675496
3130628703130628704CCT2GENICheterozygous57675501
3130628756130628757CT18GENIChomozygous57675503
3130628958130628959AG6GENICheterozygous57675505
3130629430130629431TC20GENIChomozygous57675508
3130630314130630316TA--4GENICheterozygous57675513
3130630672130630673AG18GENICpossibly homozygous57675515
3130631056130631057GA24GENIChomozygous57675517
3130632053130632054TC21GENICpossibly homozygous57675519
3130632109130632110GA16GENICpossibly homozygous57675521
3130632212130632213AG25GENIChomozygous57675523
3130633317130633318CT18GENIChomozygous57675526
3130633845130633846CT15GENIChomozygous57675529
3130635567130635568TTTG14GENICpossibly homozygous57675535