chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1245482925245482926TG40GENIChomozygous108599045
1245484534245484535CT29GENICpossibly homozygous109208408
1245487458245487459GA32GENIChomozygous108599054
1245488527245488528TC44GENIChomozygous109208410
1245496180245496181GA56GENICheterozygous108599069
1245496221245496222AG50GENICheterozygous108599071
1245502085245502086AG42GENIChomozygous109208418
1245513087245513088GC24GENIChomozygous108599112
1245514258245514259TC29GENIChomozygous108599114
1245515748245515749AG25GENIChomozygous108599116
1245516179245516180AG35GENIChomozygous108599118
1245497407245497408AG61GENICheterozygous109372760
1245498763245498764GA27GENICheterozygous109372762