chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135592789955927900AG21GENICpossibly homozygous49762865
135592796455927965TC30GENIChomozygous49762866
135592828955928290TC13GENICheterozygous49762867
135592876055928790ACTCCAGGTCTTTGGGAGAATCATCTCTGA------------------------------1GENIChomozygous49762868
135592884855928849GA14GENIChomozygous49762869
135593049255930493AAC7GENIChomozygous49762870
135593050455930505AG6GENIChomozygous49762871
135593051055930511AG6GENICheterozygous49762872
135593103955931040C-10GENICpossibly homozygous49762873
135593278455932792CACGCACG--------8GENIChomozygous49762874
135593283755932838TTCA10GENIChomozygous49762876
135593511955935120TC18GENICpossibly homozygous49762879
135593517655935177GA13GENIChomozygous49762880
135593532955935330AG16GENICpossibly homozygous49762881
135593534955935361CTCTGCACCCAC------------1GENIChomozygous49762882
135593567455935675GT23GENICpossibly homozygous49762883
135593576855935769TC13GENIChomozygous49762884
135593588155935882CT14GENICheterozygous49762885
135593597155935972GA22GENICpossibly homozygous49762886
135593619355936194TC11GENIChomozygous49762888
135593663155936632AG19GENIChomozygous49762891
135593698955936990GGC11GENIChomozygous49762892
135593733555937336AG3GENIChomozygous49762893