chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
96678865866788659AG23GENIChomozygous117370026
96678895266788953AG16GENIChomozygous117370030
96678978666789787AG16GENIChomozygous117370038
96679234966792350CT25GENIChomozygous117370056
96679347066793471GA16GENIChomozygous117370068
96679310366793104TC32GENICheterozygous117824344
96679312466793125AT27GENICheterozygous117824346
96679310666793107TA28GENICheterozygous117875936
96680061566800616AG21GENIChomozygous117370106
96680109066801091GA33GENIChomozygous117370108
96680219366802194TG23GENIChomozygous117370112
96680219566802196AG25GENIChomozygous117370114
96680503566805036AG19GENIChomozygous117370128
96681102366811024TC16GENIChomozygous117370144
96680129166801292CT21GENIChomozygous117711139
96680133666801337GA29GENIChomozygous117711141
96680137566801376CG25GENIChomozygous117711143
96680553666805537TG10GENIChomozygous117711145
96681234966812350AG14GENICheterozygous120269289
96682461566824616CG27GENIChomozygous117711147
96682719566827196AG20GENIChomozygous117370203
96682902666829027GA48GENICheterozygous120269290
96682911066829111TA65GENICheterozygous120269291
96683089066830891CT20GENICheterozygous117824349
96683330566833306CA248GENICheterozygous120269292
96683414966834150GA61GENICheterozygous120269293
96683461766834618GT34GENICheterozygous117875943
96683462666834627AG31GENICheterozygous117798782
96683465266834653CT27GENICheterozygous117798783
96683466266834663GT25GENICheterozygous117798784
96683466966834670CT22GENICheterozygous117798785
96683508266835083CA36GENICheterozygous120269294
96683509466835095TC39GENICheterozygous120269295
96683510566835106GC35GENICheterozygous120269296
96683523466835235TC19GENICheterozygous117370251
96683525566835256GA15GENICpossibly homozygous117824356
96683890866838909GA18GENICpossibly homozygous117824357
96684017166840172TC28GENIChomozygous117711149
96684318166843182AG26GENIChomozygous117370286
96684387566843876CT22GENIChomozygous117824358
96684452766844528GT23GENIChomozygous117370298