chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1146961403146961404AG11GENIChomozygous60886315
1146962208146962209GA14GENIChomozygous60886316
1146962854146962855CT17GENIChomozygous60886317
1146963663146963664TA10GENIChomozygous60886318
1146964040146964041GA14GENIChomozygous60886320
1146964117146964118TC15GENIChomozygous60886322
1146964500146964501AAT9GENIChomozygous60886323
1146964524146964525AG16GENIChomozygous60886324
1146965288146965289GA12GENIChomozygous62164405
1146965290146965292GA--12GENIChomozygous60886325
1146966159146966160AT8GENIChomozygous60886327
1146966227146966232GGGGT-----9GENIChomozygous60886328
1146966596146966597TA9GENIChomozygous60886329
1146966855146966856TC8GENIChomozygous60886330
1146967472146967473GA15GENIChomozygous60886331
1146967768146967769AG11GENIChomozygous60886332
1146968072146968073TC14GENIChomozygous60886333
1146968077146968078CT14GENIChomozygous60886334
1146968155146968159TATT----20GENIChomozygous60886335
1146968444146968445GA14GENIChomozygous60886336
1146969722146969723AAGCTAC15GENIChomozygous60886339
1146969843146969847CTCT----11GENIChomozygous60886340
1146970257146970258AAT11GENIChomozygous60886342
1146970691146970692CT15GENIChomozygous60886343
1146971220146971221GA13GENIChomozygous60886344
1146971401146971402GA19GENIChomozygous60886345
1146971549146971550GC19GENIChomozygous60886346