chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
171803019518030196AG16GENIChomozygous125499882
171803377618033777AT14GENIChomozygous125499883
171803380518033806CT13GENIChomozygous110976375
171803416918034170CT8GENIChomozygous110976377
171803502718035028GA8GENIChomozygous110976379
171803549118035492GA24GENIChomozygous110976381
171803678018036781GA17GENIChomozygous110976383
171803900718039008AT10GENIChomozygous110976385
171804035218040353AG7GENICheterozygous119332084
171804066018040661GA24GENIChomozygous110976387
171804080018040801CA11GENIChomozygous110976389
171804175218041753TC22GENIChomozygous110976391
171804299118042992GA17GENIChomozygous110976393
171804312018043121CT11GENIChomozygous111175398
171804341918043420GA14GENIChomozygous110976395
171804346118043462TC18GENIChomozygous110976397
171804357018043571CT17GENIChomozygous110976399
171804419018044191TA21GENIChomozygous110976405
171804460118044602TC7GENIChomozygous110976407
171804464918044650TC22GENIChomozygous110976409
171804491818044919TA17GENIChomozygous110976411
171804496718044968GT17GENIChomozygous110976413
171804506718045068CT15GENIChomozygous110976415
171804533818045339GA12GENIChomozygous110976417
171804537118045372TC14GENIChomozygous110976419
171804673818046739CG16GENIChomozygous110976421
171804686818046869AG13GENIChomozygous110976425
171804726418047265TC24GENIChomozygous110976427
171804732218047323GA12GENIChomozygous110976429