chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4157182273157182274GA29GENIChomozygous113184463
4157183479157183480TC32GENIChomozygous112905781
4157184151157184152GC35GENIChomozygous112905783
4157184417157184418CA22GENIChomozygous112905785
4157185982157185983AG33GENIChomozygous112905789
4157187422157187423CT25GENIChomozygous112905797
4157187489157187490AG45GENIChomozygous112905799
4157187751157187752GT30GENIChomozygous112905801
4157188600157188601CT36GENIChomozygous112905803
4157188822157188823AG40GENIChomozygous112905807
4157189364157189365TC39GENIChomozygous112905809
4157189489157189490GA36GENIChomozygous113184464
4157189773157189774GC33GENIChomozygous112905811
4157190510157190511CT22GENIChomozygous113184465
4157191167157191168GA35GENIChomozygous113184466
4157191492157191493GA17GENIChomozygous112905815
4157191803157191804TA27GENICpossibly homozygous113184467
4157193291157193292TC15GENIChomozygous112905817
4157199738157199739TC36GENIChomozygous112905823
4157201002157201003CT32GENIChomozygous112905825
4157201757157201758TG23GENIChomozygous113184470
4157202472157202473GA24GENIChomozygous113184471
4157203621157203622AG27GENIChomozygous112905831
4157205778157205779TC19GENIChomozygous112905833
4157206463157206464CT18GENIChomozygous113184472
4157208004157208005GA27GENIChomozygous113184473
4157208244157208245GA28GENIChomozygous113184474
4157208325157208326CA27GENICpossibly homozygous113184475
4157208495157208496AG26GENIChomozygous112905839
4157208578157208579GA29GENIChomozygous113184476
4157209553157209554AC25GENIChomozygous112905841
4157210422157210423TC11GENIChomozygous112905843
4157210693157210694CA13GENIChomozygous112905845
4157211953157211954AG15GENIChomozygous113184477
4157215447157215448AG29GENIChomozygous112905849
4157215880157215881AG38GENIChomozygous112905851
4157216137157216138TC37GENIChomozygous112905853
4157216381157216382CT20GENIChomozygous112905859
4157219813157219814CT18GENIChomozygous113184478
4157221183157221184AG29GENIChomozygous112905867