chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1100434622100434623CG25GENIChomozygous109046547
1100434823100434824AG22GENIChomozygous108898988
1100435071100435072TC27GENIChomozygous108898990
1100435855100435856AG27GENIChomozygous108898991
1100435958100435959AG34GENIChomozygous108898993
1100436100100436101AG30GENIChomozygous109046548
1100438347100438348GT38GENIChomozygous108898994
1100439848100439849GA23GENIChomozygous108898996
1100440583100440584CT20GENIChomozygous108898997
1100441195100441196CT37GENIChomozygous108898999
1100441808100441809AG25GENIChomozygous108899000
1100442058100442059TG30GENIChomozygous108899001
1100443036100443037TG33GENIChomozygous108899003
1100446164100446165AG31GENIChomozygous108899006
1100448129100448130AG21GENIChomozygous108899007
1100448444100448445GA25GENIChomozygous108899009
1100448640100448641AG24GENIChomozygous108899010
1100449104100449105CT36GENIChomozygous108899012
1100449307100449308AG39GENIChomozygous108899013
1100449670100449671CG34GENIChomozygous108899015
1100449960100449961TG30GENIChomozygous108899016
1100450241100450242GA29GENIChomozygous108899018
1100450292100450293GA30GENIChomozygous108899019
1100450592100450593TC42GENIChomozygous108899020
1100451823100451824AG30GENIChomozygous108899022
1100455358100455359AG32GENIChomozygous108899023
1100456608100456609GA23GENIChomozygous108899025
1100458244100458245CA32GENIChomozygous108899026
1100458661100458662GA33GENIChomozygous108899028
1100459372100459373GA29GENICpossibly homozygous108899029
1100459473100459474AG35GENICheterozygous108899031
1100460699100460700AG25GENIChomozygous108899032
1100463218100463219GC41GENICpossibly homozygous108899034
1100464182100464183CA33GENICheterozygous109046549
1100465722100465723AG36GENIChomozygous108899035
1100466335100466336AG36GENIChomozygous108899037
1100468227100468228CT30GENIChomozygous108899038
1100457732100457733AG73GENIChomozygous108164971
1100457918100457919GT10GENIChomozygous108164972
1100457919100457920GA10GENIChomozygous108164973