chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5111817554111817555TC18GENIChomozygous55640419
5111818340111818341AG12GENIChomozygous55640420
5111819025111819026C-15GENIChomozygous55640421
5111819498111819499GC26GENIChomozygous55640422
5111820710111820712TA--5GENIChomozygous55640423
5111820965111820966GGTTTT6GENIChomozygous55640424
5111820978111820979TTTG4GENIChomozygous56550444
5111821143111821144AG18GENIChomozygous55640425
5111822589111822590CT18GENIChomozygous55640426
5111822983111822985TT--8GENIChomozygous55640427
5111823630111823632TT--12GENICheterozygous56120374
5111823631111823632T-12GENICheterozygous56051961
5111823727111823728TC22GENIChomozygous55640428
5111824018111824019GGT20GENICpossibly homozygous55640429
5111824295111824296TG6GENIChomozygous55640432
5111824411111824412TTTGTG15GENIChomozygous55640433
5111825013111825014CT5GENIChomozygous55640434