chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
105566979955669800CT37GENIChomozygous51890350
105567169655671697TTA13GENICheterozygous51459887
105567339155673392CCTT8GENICpossibly homozygous51653464
105567341655673417CT22GENICheterozygous51890354
105567419355674194AC39GENIChomozygous51653466
105567575955675760TC30GENIChomozygous51653468