chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
4155681820155681821TTA13GENIChomozygous58089381
4155683619155683620GC23GENIChomozygous58089383
4155683941155683942CCGGG9GENIChomozygous58089385
4155685385155685386GT12GENIChomozygous58089389
4155686017155686018AG31GENIChomozygous57526714
4155686660155686661AT18GENIChomozygous58089391
4155687107155687108TG15GENIChomozygous58089393
4155688536155688537GGTTTT20GENIChomozygous57526724
4155688566155688567GGTTA31GENICpossibly homozygous58287271
4155688620155688621GA36GENIChomozygous58089395
4155688894155688899GGTTC-----30GENIChomozygous57526730
4155688958155688959GC37GENIChomozygous58089397
4155689322155689323AC11GENIChomozygous57526740
4155690734155690735CG27INTERGENIChomozygous58089399
4155690760155690761CT25INTERGENIChomozygous58089401
4155691021155691022T-9INTERGENIChomozygous58089403
4155688537155688538GT20GENIChomozygous58348313