chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
135592789955927900AG38GENIChomozygous528446305
135592796455927965TC32GENIChomozygous531888331
135592828955928290TC33GENIChomozygous528446306
135592876055928790ACTCCAGGTCTTTGGGAGAATCATCTCTGA------------------------------12GENIChomozygous694562106
135592884855928849GA11GENIChomozygous528446307
135593049255930493AAC18GENIChomozygous694562107
135593050455930505AG22GENIChomozygous531888332
135593051055930511AG23GENIChomozygous531888333
135593103955931040C-24GENIChomozygous694562108
135593278455932792CACGCACG--------15GENIChomozygous694562109
135593279955932800GA21GENICheterozygous531888334
135593283755932838TTCA26GENIChomozygous694562111
135593424455934245GGCC7GENIChomozygous694562112
135593425555934256TC25GENIChomozygous528446308
135593511955935120TC35GENIChomozygous528446309
135593517655935177GA32GENIChomozygous531888335
135593532955935330AG19GENIChomozygous528446310
135593534955935361CTCTGCACCCAC------------11GENIChomozygous694562113
135593567455935675GT21GENIChomozygous528446311
135593576855935769TC25GENIChomozygous528446312
135593588155935882CT24GENIChomozygous528446313
135593597155935972GA27GENIChomozygous528446314
135593615555936156TTACACAC1GENIChomozygous694562115
135593619355936194TC15GENICpossibly homozygous528446315
135593640055936402TT--18GENICpossibly homozygous694562116
135593640155936402T-18GENICheterozygous694562118
135593663155936632AG36GENIChomozygous528446316
135593698955936990GGC19GENIChomozygous694562119
135593733555937336AG28GENIChomozygous528446317
135593735355937360GGGCTCC-------11GENIChomozygous694562120
135593736155937362GA18GENICheterozygous531888336
135593736855937369GA20GENICheterozygous531888337