chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5135631590135631592GT25GENICheterozygous141002754
5135661640135661641CT18GENIChomozygous137630118
5135747675135747677AT19GENICheterozygous141002755
5135792949135792950CG11GENICpossibly homozygous137630270
5135814885135814886G27GENICheterozygous403159336
5135672488135672489GT17GENICheterozygous403159319
5135672488135672489G17GENIChomozygous403159320
5135814885135814886GC27GENICheterozygous403159337
5135815908135815909A42GENIChomozygous403159345
5135815908135815909AG42GENICheterozygous403159346
5135822079135822080C17GENICheterozygous403821659
5135834910135834911T9GENIChomozygous137343924
5135834919135834919T10GENIChomozygous137343925
5135843861135843862A32GENICheterozygous403159358
5135843861135843862AT32GENICheterozygous403159359
5135888839135888839A36GENICheterozygous140884137
5135917006135917007TA17GENIChomozygous403159371
5135917006135917007T17GENICheterozygous403159372
5135934909135934910TA22GENICheterozygous403159376
5135934909135934910T22GENICheterozygous403159377
5135822079135822080CA17GENICheterozygous141116556