chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47875012878750129GC16GENIChomozygous112739081
47875015578750156GC13GENIChomozygous113353202
47877620378776204TC19GENIChomozygous119584893
47875776578757766A19GENICheterozygous131354282
47876806478768065TC21GENIChomozygous119517366
47877866978778670CT19GENIChomozygous119517368
47878641078786411TC17GENIChomozygous112739236
47879177878791779CT11GENIChomozygous112739296
47879191278791913CG17GENIChomozygous112739298
47880676578806766AT25GENIChomozygous112739396
47882117278821173A13GENICheterozygous128052303
47883677378836773GA6GENIChomozygous128052312
47883682178836821AGC7GENIChomozygous128052313
47883943378839433T15GENIChomozygous128052315
47883945578839456AC15GENIChomozygous112739575
47884550278845503AG18GENIChomozygous112739603
47884679878846799GC20GENIChomozygous128128499
47884680078846801TC19GENIChomozygous128128500
47884681178846812TG21GENIChomozygous128128501
47884681778846818GT22GENIChomozygous128128502
47884681978846820GT22GENIChomozygous128128503
47884684478846844TTG16GENIChomozygous128052323
47884680478846808TTTT19GENIChomozygous128052319
47884680978846809AGCC19GENIChomozygous128052320
47884682578846834CCGGAGGGG20GENIChomozygous128052321
47884683878846839T18GENIChomozygous128052322
47884491978844919T18GENICheterozygous129902755
47884685478846854G20GENIChomozygous128052324
47884685578846855TTTAA20GENIChomozygous128052325
47884686478846865GT18GENIChomozygous112739617
47884687078846871AC18GENIChomozygous112739619
47885278878852789GA14GENIChomozygous119517370
47885809678858099GCC18GENIChomozygous128052331
47885877178858771CTA18GENIChomozygous128052332
47887041578870415T26GENIChomozygous131354283
47887878778878788G20GENIChomozygous128052340