chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
8131090612131090613TC35GENIChomozygous52896194
8131091216131091217TC40GENIChomozygous53065537
8131093978131093979GC56GENIChomozygous52896204
8131094058131094059AG59GENIChomozygous52896207
8131096777131096778GC158GENICheterozygous53172561
8131096887131096888TC182GENICheterozygous52896224
8131097814131097815TA224GENICheterozygous52896230
8131097822131097823CG212GENICheterozygous52896232
8131097851131097852CG211GENICheterozygous52896236
8131097827131097828TA222GENICheterozygous52896234
8131097872131097873CT198GENICheterozygous52896239
8131097878131097879CT189GENICheterozygous52896242
8131097887131097888AT189GENICheterozygous53065538
8131097889131097890CT178GENICheterozygous53293101
8131098057131098058CA181GENICpossibly homozygous52896244
8131098060131098061GA189GENICheterozygous53065539
8131098282131098283CT188GENICheterozygous53065540
8131098392131098393TA171GENICheterozygous53065541
8131100021131100022TA65GENICheterozygous53065547
8131098487131098488TC160GENICheterozygous53065542
8131099419131099420GC115GENICpossibly homozygous53065545
8131099986131099987GA77GENIChomozygous53065546
8131100087131100088AG55GENICpossibly homozygous53065549
8131100123131100124GA52GENIChomozygous53065550
8131100129131100130GT56GENIChomozygous53065551
8131100794131100795TC91GENICheterozygous53065552
8131101188131101189AC67GENICpossibly homozygous53065553
8131101237131101238AC73GENICpossibly homozygous53065554
8131101301131101302CT48GENICheterozygous52896296
8131101306131101307GC46GENICheterozygous52896299
8131103227131103228TC51GENIChomozygous53065555
8131103302131103303TC43GENIChomozygous53065556
8131103494131103495CG42GENIChomozygous53065557
8131104227131104228CA40GENIChomozygous53065558
8131104625131104626TG56GENIChomozygous53065559
8131104824131104826GT--7GENIChomozygous52896310
8131105633131105634TC58GENIChomozygous52896315