chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5129512506129512507A31GENICpossibly homozygous137341070
5129512999129513000G48GENIChomozygous137341071
5129515341129515342CT41GENIChomozygous137620184
5129520105129520106GA50GENIChomozygous137620185
5129520490129520491CT41GENIChomozygous137620186
5129526131129526132T11GENIChomozygous137341072
5129526149129526150TC11GENICheterozygous141004680
5129526150129526151TC11GENICheterozygous137620187
5129527237129527238GA50GENIChomozygous137620189
5129528456129528456AC51GENICpossibly homozygous137341073
5129528501129528502TG50GENICpossibly homozygous137620190
5129531911129531912GA42GENIChomozygous137620191