chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
47875776578757766A15GENICheterozygous131354282
47883354578833546A10GENICheterozygous131641047
47883677378836773GA5GENIChomozygous128052312
47883682178836821AGC6GENIChomozygous128052313
47883943378839433T18GENIChomozygous128052315
47883945578839456AC22GENIChomozygous112739575
47884680978846809AGCC27GENIChomozygous128052320
47884681178846812TG24GENIChomozygous128128501
47884681778846818GT23GENIChomozygous128128502
47884681978846820GT22GENIChomozygous128128503
47884682578846834CCGGAGGGG22GENIChomozygous128052321
47884683878846839T20GENIChomozygous128052322
47884684478846844TTG20GENIChomozygous128052323
47884685478846854G18GENIChomozygous128052324
47884685578846855TTTAA18GENIChomozygous128052325
47884686478846865GT22GENIChomozygous112739617
47884687078846871AC22GENIChomozygous112739619
47885809678858099GCC21GENIChomozygous128052331
47885877178858771CTA18GENIChomozygous128052332
47887878778878788G13GENIChomozygous128052340
47886452778864528CG13GENIChomozygous131644600