chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1146961403146961404AG45GENIChomozygous60886315
1146962208146962209GA24GENIChomozygous60886316
1146962378146962379T-17GENIChomozygous61677774
1146962854146962855CT59GENIChomozygous60886317
1146963663146963664TA34GENIChomozygous60886318
1146963696146963697CCACACACACAGAGAGAG17GENICheterozygous60886319
1146963696146963697CCACACACAGAGAGAG17GENICheterozygous62164403
1146964040146964041GA15GENIChomozygous60886320
1146964050146964051TA11GENICpossibly homozygous60886321
1146964117146964118TC14GENIChomozygous60886322
1146964500146964501AAT34GENIChomozygous60886323
1146964524146964525AG33GENIChomozygous60886324
1146965288146965289GA36GENIChomozygous62164405
1146965290146965292GA--37GENIChomozygous60886325
1146966159146966160AT10GENIChomozygous60886327
1146966227146966232GGGGT-----3GENIChomozygous60886328
1146966596146966597TA26GENIChomozygous60886329
1146966855146966856TC33GENIChomozygous60886330
1146967472146967473GA32GENIChomozygous60886331
1146967768146967769AG35GENIChomozygous60886332
1146968072146968073TC18GENIChomozygous60886333
1146968077146968078CT18GENIChomozygous60886334
1146968155146968159TATT----24GENIChomozygous60886335
1146968444146968445GA40GENIChomozygous60886336
1146969722146969723AAGCTAC36GENIChomozygous60886339
1146969843146969847CTCT----27GENIChomozygous60886340
1146969992146969993T-25GENIChomozygous60886341
1146970257146970258AAT31GENIChomozygous60886342
1146970691146970692CT23GENIChomozygous60886343
1146971220146971221GA43GENIChomozygous60886344
1146971401146971402GA31GENIChomozygous60886345
1146971549146971550GC31GENIChomozygous60886346