chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
7132471537132471538CT53GENIChomozygous133409109
7132573068132573069GA8GENICheterozygous133185411
7132616931132616932GC43GENICheterozygous130768818
7132587385132587385GTTTGTTTGATTTGGTTGGTTGGTTTGGTTGGTTTGGTTGGTTGGTTGGTTTGGTTG5GENICheterozygous133406658
7132617272132617273GA56GENICheterozygous115902789
7132617405132617406AT18GENICheterozygous122864270
7132617989132617990AG3GENICheterozygous133409110
7132623035132623036GT24GENICheterozygous122864279
7132623036132623037CA24GENICheterozygous122864280
7132626631132626631AC16GENICpossibly homozygous130346799
7132627173132627174GA42GENICheterozygous116088896
7132627174132627175AG42GENICheterozygous130566701
7132627184132627185CA41GENICheterozygous116088898
7132627190132627191CA43GENICheterozygous128563349
7132627191132627192AG44GENICheterozygous128563350
7132627216132627217GA44GENICheterozygous116088900
7132645486132645487GA71GENICheterozygous115902867
7132645491132645492CT68GENICheterozygous115902869
7132645581132645582T58GENICheterozygous128521991
7132645583132645586TCT59GENICheterozygous128521992
7132645589132645590CT56GENICheterozygous122864304
7132645593132645594GC53GENICheterozygous122912421
7132645600132645601CT52GENICheterozygous122912422
7132645997132645998AG52GENICheterozygous130566704
7132646019132646020TG53GENICheterozygous131040576
7132646025132646026CT50GENICheterozygous131040577
7132655087132655088TC7GENICheterozygous128563353
7132658118132658119GT10GENICheterozygous116304601
7132727790132727792AC31GENICheterozygous130765517