chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
34633021546330216TA41GENIChomozygous978516243
34635100646351007AG4GENIChomozygous978516244
34635110646351107TG24GENIChomozygous978516245
34635124846351249AG33GENIChomozygous978516246
34635134346351344GA39GENIChomozygous978516247
34635158246351583GT35GENIChomozygous978516248
34635180346351804TC30GENIChomozygous978516249
34635188546351886TC29GENIChomozygous978516250
34635227046352271TC21GENIChomozygous978516251
34635237046352371AG45GENIChomozygous978516252
34635238046352381AC42GENIChomozygous978516253
34635252746352528AC32GENIChomozygous978516254
34635253846352539TC30GENIChomozygous978516255
34635268146352682TC17GENIChomozygous978516256
34635269146352692CT16GENIChomozygous978516257
34635287146352872GA39GENIChomozygous978516258
34635317446353175AG29GENIChomozygous978516259
34635340346353404GC37GENIChomozygous978516260
34635367746353678TC25GENIChomozygous978516261
34635415546354156CT26GENIChomozygous978516262
34635620846356209GA37GENIChomozygous978516263
34635826746358268CT12GENIChomozygous978516264
34635995046359951CG57GENIChomozygous978516265
34636006946360070CG19GENIChomozygous978516266