chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77127624971276250TC24GENIChomozygous115710141
77127706171277062AG35GENIChomozygous116191260
77127752971277530AG43GENIChomozygous116191262
77127763071277631TC35GENIChomozygous115710142
77127768471277685AC41GENIChomozygous115710144
77127860971278610GA35GENIChomozygous116191264
77127876671278767CT30GENIChomozygous116191266
77127884471278845TC28GENIChomozygous116191268
77127903071279031TC36GENIChomozygous116191270
77127917671279177AG40GENIChomozygous116191272
77127951171279512TC27GENIChomozygous116191274
77127960671279607TC22GENIChomozygous116191276
77127994371279944CA32GENIChomozygous116191278
77128007571280076CT42GENIChomozygous116191280
77128093071280931CT36GENIChomozygous116191286
77128149971281500AG24GENIChomozygous116191288
77128191871281919TC18GENIChomozygous116191290
77128194671281947TC18GENIChomozygous116191292
77128250571282506TC20GENIChomozygous116191294
77128254271282543AC20GENIChomozygous116191296
77128254371282544GT19GENIChomozygous116191298
77128297571282976TC23GENIChomozygous116191300
77128324671283247AG14GENIChomozygous116191302
77128469371284694CT44GENIChomozygous116191310
77128492171284922TC26GENIChomozygous116191312
77128516671285167AG25GENIChomozygous116191314
77128519671285197AT27GENIChomozygous116191316
77128603571286036CA38GENIChomozygous116191318
77128611071286111TA48GENIChomozygous116191320
77128662171286622TA29GENIChomozygous116191322
77128665371286654GA27GENIChomozygous115710146
77128666771286668GA26GENIChomozygous116191324
77128669071286691GT27GENIChomozygous116191326
77128687971286880TG26GENIChomozygous116191328
77128700671287007TG27GENIChomozygous116191330
77128783971287840TC26GENIChomozygous116191332
77128827271288273TC21GENIChomozygous116191334
77128900271289003TC31GENIChomozygous116191336
77129350071293501AG17GENIChomozygous116191340
77129353671293537GA15GENIChomozygous116191342