chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55951315359513154AC48GENIChomozygous113821725
55951350059513501AG46GENIChomozygous113821727
55951376159513762TC44GENIChomozygous113821729
55951518059515181TC48GENIChomozygous113821731
55951595759515958GA42GENIChomozygous113821733
55951704859517049GA36GENIChomozygous113821735
55951759459517595GT56GENIChomozygous113821737
55951763459517635AT35GENIChomozygous113821739
55951854159518542GT27GENIChomozygous113821741
55951887659518877CT30GENIChomozygous113821743
55951977359519774CT31GENIChomozygous113821747
55952001059520011CT50GENIChomozygous113821749
55952011659520117TC50GENIChomozygous113821751
55952057759520578GA37GENIChomozygous113821753
55952200259522003CA46GENIChomozygous113821757
55952209659522097GT29GENIChomozygous113821759
55952294859522949CT49GENICpossibly homozygous113821777
55952304459523045GT31GENIChomozygous113821779
55952311559523116TC35GENIChomozygous113821781
55952393159523932TA45GENIChomozygous113821783
55953009559530096CG27GENIChomozygous113821789
55953519359535194AG28GENIChomozygous113821793
55953522259535223TC28GENIChomozygous113821795
55953529559535296AC32GENIChomozygous114118396
55953529659535297GA32GENIChomozygous114118398
55953595759535958AT51GENIChomozygous113821797
55953957959539580AG33GENIChomozygous113821801
55954104459541045TC42GENIChomozygous113821803
55955005959550060AG43GENIChomozygous113821807
55955058259550583AG60GENIChomozygous113821809
55955246959552470AT34GENIChomozygous113821811
55955260859552609TA53GENIChomozygous113821813