chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135592789955927900AG15GENIChomozygous565334426
135592794255927943TC24GENIChomozygous565334427
135592828955928290TC17GENIChomozygous565334428
135592875555928756CT25GENIChomozygous565334429
135592948255929483GA21GENIChomozygous565334430
135593071755930718GT19GENIChomozygous565334431
135593103955931040C-5GENIChomozygous708995543
135593200855932009CT23GENIChomozygous565334432
135593259155932592AG9GENIChomozygous565334433
135593278355932784AACACG13GENIChomozygous708995545
135593283755932838TTCA23GENIChomozygous708995546
135593293055932948CACACACACGCACGCACG------------------10GENICpossibly homozygous708995547
135593424455934245GGC3GENIChomozygous708995548
135593483655934837CT13GENIChomozygous565334434
135593511955935120TC17GENIChomozygous565334435
135593532955935330AG12GENIChomozygous565334436
135593534955935361CTCTGCACCCAC------------9GENIChomozygous708995549
135593567455935675GT13GENIChomozygous565334437
135593576855935769TC25GENIChomozygous565334438
135593588155935882CT10GENIChomozygous565334439
135593597155935972GA13GENIChomozygous565334440
135593615555936156TTACAC5GENIChomozygous708995551
135593619355936194TC16GENIChomozygous565334441
135593639955936402TTT---15GENICheterozygous708995554
135593640055936402TT--15GENICpossibly homozygous708995555
135593640155936402T-15GENICheterozygous708995556
135593652655936527GA14GENIChomozygous565334442
135593663155936632AG11GENIChomozygous565334443
135593732055937321GA10GENIChomozygous565334444
135593733555937336AG8GENIChomozygous565334445
135593735355937360GGGCTCC-------7GENIChomozygous708995557
135593736855937369GA6GENIChomozygous568317565
135593799155937992TTCACACA4GENIChomozygous708995559
135593859455938595CT22GENIChomozygous565334446