chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
77106534971065350AG47GENICheterozygous115709437
77106537271065373GA51GENICheterozygous128554827
77106574971065750CT72GENICheterozygous116033781
77106579871065799TC83GENICheterozygous115709441
77106596871065969TC104GENICheterozygous116033783
77106602171066022CT72GENICheterozygous116033785
77106604271066043AG62GENICheterozygous116033787
77106619871066199TC53GENICheterozygous115709442
77106620771066208CT56GENICheterozygous115709443
77106632171066322GA102GENICheterozygous115709445
77106633571066336T96GENICheterozygous128478173
77106637071066371TC85GENICheterozygous115709447
77106638471066385GA75GENICheterozygous115709448
77106639571066396TC65GENICheterozygous115709449
77106645171066452G34GENICheterozygous128478174
77106645271066453TC34GENICheterozygous122796810
77106645671066456C31GENICheterozygous128478175
77106646871066469AC27GENICheterozygous115709450
77106648371066484CT28GENICheterozygous115709451
77106649171066492TA29GENICheterozygous115709452
77106649671066497AT28GENICheterozygous115709453
77106650571066506AT27GENICheterozygous115709454
77106702971067031CC3GENICheterozygous128478176
77106703371067043GCCTAACTCG3GENICheterozygous128478177
77106709471067095TG2GENIChomozygous115709456
77106715671067157CG2GENIChomozygous129945367
77106842371068424CT89GENICheterozygous115709460
77106932171069322AG93GENICheterozygous116033789
77107004671070047AG107GENICheterozygous115709465
77107007071070071CT107GENICheterozygous116033791
77107014771070148AG96GENICheterozygous115709466
77107027171070272TG96GENICheterozygous115709467
77107027771070278GA93GENICheterozygous115709468
77107028071070281GT91GENICheterozygous115709469
77107148471071485CT105GENICheterozygous115709474
77107170071071701CT118GENICheterozygous115709476
77107194671071947GC107GENICheterozygous115709477
77106616471066166AT23GENICheterozygous130343843
77106785471067854T9GENICheterozygous130343844
77107066871070670TA56GENICheterozygous131679028