chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
55951315359513154AC26GENIChomozygous113821725
55951350059513501AG22GENIChomozygous113821727
55951376159513762TC29GENIChomozygous113821729
55951518059515181TC28GENIChomozygous113821731
55951595759515958GA40GENIChomozygous113821733
55951704859517049GA34GENIChomozygous113821735
55951759459517595GT23GENIChomozygous113821737
55951763459517635AT23GENIChomozygous113821739
55951854159518542GT21GENIChomozygous113821741
55951887659518877CT22GENIChomozygous113821743
55951977359519774CT31GENIChomozygous113821747
55952001059520011CT38GENIChomozygous113821749
55952011659520117TC31GENIChomozygous113821751
55952057759520578GA25GENIChomozygous113821753
55952170259521703TC24GENIChomozygous113821755
55952200259522003CA24GENIChomozygous113821757
55952209659522097GT27GENIChomozygous113821759
55952294859522949CT16GENIChomozygous113821777
55952304459523045GT19GENIChomozygous113821779
55952311559523116TC17GENIChomozygous113821781
55952393159523932TA17GENIChomozygous113821783
55952544759525448CT16GENIChomozygous113821787
55953009559530096CG31GENIChomozygous113821789
55953183459531835AG23GENIChomozygous113821791
55953522259535223TC15GENIChomozygous113821795
55953529559535296AC22GENIChomozygous114118396
55953529659535297GA22GENIChomozygous114118398
55953595759535958AT39GENICpossibly homozygous113821797
55953957959539580AG23GENIChomozygous113821801
55954104459541045TC44GENIChomozygous113821803
55955005959550060AG46GENIChomozygous113821807
55955058259550583AG35GENIChomozygous113821809
55955246959552470AT19GENIChomozygous113821811
55955260859552609TA19GENIChomozygous113821813