chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55951315359513154AC15GENIChomozygous113821725
55951350059513501AG16GENIChomozygous113821727
55951376159513762TC31GENIChomozygous113821729
55951518059515181TC8GENIChomozygous113821731
55951595759515958GA14GENIChomozygous113821733
55951704859517049GA23GENIChomozygous113821735
55951759459517595GT11GENIChomozygous113821737
55951763459517635AT9GENIChomozygous113821739
55951854159518542GT22GENIChomozygous113821741
55951887659518877CT20GENIChomozygous113821743
55951977359519774CT17GENIChomozygous113821747
55952001059520011CT19GENIChomozygous113821749
55952011659520117TC19GENIChomozygous113821751
55952057759520578GA19GENIChomozygous113821753
55952200259522003CA27GENIChomozygous113821757
55952209659522097GT25GENIChomozygous113821759
55952294859522949CT11GENIChomozygous113821777
55952304459523045GT9GENIChomozygous113821779
55952393159523932TA10GENIChomozygous113821783
55952544759525448CT10GENIChomozygous113821787
55953009559530096CG22GENIChomozygous113821789
55953183459531835AG13GENIChomozygous113821791
55953519359535194AG14GENIChomozygous113821793
55953522259535223TC12GENIChomozygous113821795
55953529559535296AC8GENIChomozygous114118396
55953529659535297GA8GENIChomozygous114118398
55953595759535958AT12GENIChomozygous113821797
55953957959539580AG13GENIChomozygous113821801
55954104459541045TC26GENIChomozygous113821803
55955005959550060AG36GENIChomozygous113821807
55955058259550583AG19GENIChomozygous113821809
55955246959552470AT21GENIChomozygous113821811
55955260859552609TA8GENIChomozygous113821813