chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5166161379166161380TG44GENIChomozygous775482422
5166187528166187529GA42GENICheterozygous775482423
5166187532166187533TC41GENICheterozygous775482424
5166187563166187564TC42GENICheterozygous775482425
5166187581166187582AG56GENICheterozygous775482426
5166192118166192119AG15GENIChomozygous775482427
5166192121166192122TG16GENICpossibly homozygous775482428
5166198887166198888TC38GENIChomozygous775482429
5166204251166204252CA23GENICpossibly homozygous775482430