chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122141385721413858AT30GENICheterozygous781773280
122141396121413962CA63GENICheterozygous781773281
122141403021414031TC83GENICheterozygous781773282
122141405421414055AT80GENICheterozygous781773283
122141409321414094GA75GENICheterozygous781773284
122141420621414207CT55GENICheterozygous781773285
122141438521414386CT100GENICheterozygous781773286
122141441421414415GA107GENICheterozygous781773287
122141454321414544AG113GENICheterozygous781773288
122141457321414574AC103GENICheterozygous781773289
122141478921414790CT74GENICheterozygous781773290
122141569721415698CT82GENICheterozygous781773291
122141611021416111TC76GENIChomozygous781773292
122141650621416507GA81GENICheterozygous781773293
122141651021416511CT87GENICheterozygous781773294
122141662221416623TC78GENICheterozygous781773295
122141666521416666GA80GENICheterozygous781773296
122141671621416717GA106GENICheterozygous781773297
122141688821416889AG43GENICheterozygous781773298
122141713321417134GT35GENICheterozygous781773299
122141717921417180CA45GENICheterozygous781773300
122141782221417823AG5GENIChomozygous781773301
122141813821418139AC37GENIChomozygous781773302