chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
42300499823004999AC28GENIChomozygous112547222
42300613923006140GC13GENIChomozygous112547228
42300767323007674GA25GENIChomozygous112547275
42300777523007776TG21GENIChomozygous119274247
42300794123007942AG34GENIChomozygous113255428
42300794223007943TA34GENIChomozygous113255429
42300867623008677CA35GENIChomozygous112547287
42300868323008684TC33GENIChomozygous112999707
42300868623008687GC33GENIChomozygous119303406
42300873823008739CT12GENIChomozygous113332495
42301220623012207CG24GENIChomozygous112547299
42301318223013183TG15GENIChomozygous112547307
42301349123013492CT20GENIChomozygous113332505
42301435223014353TC30GENIChomozygous113332507
42301497923014980CT36GENIChomozygous112547311
42301513423015135TC45GENIChomozygous112547313
42301568123015682CT37GENIChomozygous113332509
42301612823016129CG39GENIChomozygous112547319
42301626223016263AG30GENIChomozygous112547321
42301814223018143GA28GENIChomozygous113332511
42301868623018687GT40GENIChomozygous112999708
42302124723021248TG21GENIChomozygous112547337
42302193223021933TG25GENIChomozygous112547339
42302292223022923AT15GENICheterozygous119423284
42302321423023215CA37GENIChomozygous113332513
42300768323007684AT26GENIChomozygous119475660
42302448323024484GA34GENIChomozygous113332515
42302449723024498TC30GENIChomozygous112547349
42302591423025915TA13GENIChomozygous113332517
42302739623027397AG33GENIChomozygous112547357
42302793523027936TA32GENIChomozygous113087141