chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
75728302157283022AAGT2GENICheterozygous745647263
75728917957289185TCACAT------17GENICheterozygous745647264
75732086157320862GGA2GENICheterozygous745647267
75733671157336712AAC10GENIChomozygous745647268
75735915357359154A-8GENICheterozygous745647269
75740913657409137TTCA4GENIChomozygous745647272
75742574657425747GGA2GENICheterozygous745647273
75742574957425750CCA2GENICheterozygous745647274
75753131057531311GGT16GENIChomozygous745647276
75753284057532841G-8GENIChomozygous745647277
75754099657540997CA6GENICheterozygous631404293
75754601857546019G-3GENICheterozygous745647278
75754606257546063C-16GENIChomozygous745647279
75754612957546130CCA12GENICheterozygous745647280
75759951257599513GA16GENICheterozygous631404294
75760115357601154CCAA4GENICheterozygous745647281
75760904457609045T-1GENIChomozygous745647282
75762075357620755AT--8GENICheterozygous745647284
75764938157649382C-3GENIChomozygous745647285
75764938757649388GGT5GENIChomozygous745647286
75765177957651780A-8GENICheterozygous745647287
75765604057656041TTACACACACACAC10GENICheterozygous745647289
75766287057662871CCG6GENICheterozygous745647290
75767273157672732GGA2GENICheterozygous745647291
75768030857680310TC--20GENICpossibly homozygous745647292
75768920057689201A-1GENIChomozygous745647293