chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155683619155683620GC10GENIChomozygous58089383
4155685385155685386GT12GENIChomozygous58089389
4155686017155686018AG16GENICpossibly homozygous57526714
4155686660155686661AT10GENICpossibly homozygous58089391
4155687107155687108TG16GENIChomozygous58089393
4155688566155688567GGTTA7GENIChomozygous58287271
4155688620155688621GA20GENIChomozygous58089395
4155688894155688899GGTTC-----3GENIChomozygous57526730
4155688902155688905TCG---7GENICheterozygous57526734
4155688958155688959GC10GENIChomozygous58089397
4155689322155689323AC8GENIChomozygous57526740
4155690734155690735CG2INTERGENICheterozygous58089399
4155690760155690761CT13INTERGENIChomozygous58089401
4155691021155691022T-3INTERGENIChomozygous58089403