chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
122028293720282938GA13GENIChomozygous781767425
122028948620289487CT6GENIChomozygous781767426
122028949520289496GA6GENIChomozygous781767427
122028950120289502CT7GENICpossibly homozygous781767428
122028952420289525TA12GENICpossibly homozygous781767429
122028955020289551AG12GENICpossibly homozygous781767430
122029141020291411AT29GENIChomozygous781767431
122029142820291429GA29GENIChomozygous781767432
122029146320291464GC24GENIChomozygous781767433
122029149320291494GC7GENIChomozygous781767434
122029149920291500CG7GENIChomozygous781767435
122029233720292338GA10GENIChomozygous781767436
122029379520293796AC23GENIChomozygous781767437
122029379920293800TG29GENICheterozygous781767438
122029380820293809AG33GENIChomozygous781767439
122029387620293877GC76GENICheterozygous781767440
122029389020293891AT88GENICheterozygous781767441
122029389420293895TC89GENICheterozygous781767442
122029390020293901CT92GENIChomozygous781767443
122029391520293916GA98GENICheterozygous781767444
122029395420293955CA104GENICheterozygous781767445
122029396020293961AC108GENICheterozygous781767446
122029397520293976CA104GENICheterozygous781767447
122029400320294004GC92GENICheterozygous781767448
122029401920294020AT92GENICheterozygous781767449
122029404120294042CA92GENICheterozygous781767450
122029406220294063TA90GENICheterozygous781767451
122029409920294100AG74GENIChomozygous781767452
122029412420294125GA59GENICheterozygous781767453
122029414120294142TG52GENICheterozygous781767454
122029418420294185CG17GENICheterozygous781767455
122029419020294191AC12GENIChomozygous781767456
122029421820294219GC7GENICheterozygous781767457
122029441220294413CT11GENICpossibly homozygous781767458
122029441320294414GA11GENIChomozygous781767459
122029442020294421TG13GENICheterozygous781767460
122029444120294442TC10GENICheterozygous781767461