chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
2243551211243551212AG14GENIChomozygous802276239
2243551784243551785TC15GENIChomozygous802276240
2243552164243552165TC29GENIChomozygous802276241
2243552235243552236AG28GENICheterozygous802276242
2243552647243552648AG23GENIChomozygous802276243
2243553059243553060GC20GENIChomozygous802276244
2243553157243553158TG37GENIChomozygous802276245
2243553214243553215AC33GENIChomozygous802276246
2243553319243553320GA17GENIChomozygous802276247
2243553424243553425TC24GENIChomozygous802276248
2243553729243553730AG10GENIChomozygous802276249
2243554892243554893CG30GENIChomozygous802276250
2243555015243555016AG40GENICpossibly homozygous802276251
2243555276243555277TG21GENIChomozygous802276252
2243556039243556040AG10GENICpossibly homozygous802276253
2243556041243556042AG9GENICheterozygous802276254
2243556058243556059TG6GENIChomozygous802276255
2243556282243556283TG5GENICheterozygous802276256
2243556463243556464TA19GENIChomozygous802276257
2243556902243556903TC17GENIChomozygous802276258
2243557156243557157GA23GENIChomozygous802276259
2243557183243557184TC28GENIChomozygous802276260
2243557344243557345TC13GENIChomozygous802276261
2243557965243557966CT22GENICpossibly homozygous802276262
2243559046243559047GA17GENIChomozygous802276263
2243559104243559105CT20GENIChomozygous802276264
2243559231243559232CA28GENIChomozygous802276265
2243559316243559317AC15GENIChomozygous802276266
2243559682243559683CT19GENIChomozygous802276267
2243559690243559691GA19GENIChomozygous802276268
2243559982243559983CT45GENIChomozygous802276269
2243560178243560179GT27GENIChomozygous802276270
2243560446243560447TG12GENIChomozygous802276271
2243560718243560719AG9GENIChomozygous802276272
2243561110243561111AG16GENIChomozygous802276273
2243561224243561225TC21GENIChomozygous802276274
2243561420243561421AG28GENIChomozygous802276275