chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
1146961403146961404AG28GENIChomozygous60886315
1146962208146962209GA31GENIChomozygous60886316
1146962378146962379T-20GENICpossibly homozygous61677774
1146962854146962855CT36GENIChomozygous60886317
1146963663146963664TA27GENIChomozygous60886318
1146963696146963697CCACACACACAGAGAGAG8GENICheterozygous60886319
1146963696146963697CCACACACAGAGAGAG8GENICheterozygous62164403
1146964040146964041GA25GENIChomozygous60886320
1146964050146964051TA23GENICpossibly homozygous60886321
1146964117146964118TC25GENIChomozygous60886322
1146964500146964501AAT22GENIChomozygous60886323
1146964524146964525AG28GENIChomozygous60886324
1146965288146965289GA20GENIChomozygous62164405
1146965290146965292GA--21GENIChomozygous60886325
1146966159146966160AT12GENIChomozygous60886327
1146966227146966232GGGGT-----8GENIChomozygous60886328
1146966596146966597TA20GENIChomozygous60886329
1146966855146966856TC19GENIChomozygous60886330
1146967472146967473GA17GENIChomozygous60886331
1146967768146967769AG21GENIChomozygous60886332
1146968072146968073TC32GENIChomozygous60886333
1146968077146968078CT32GENIChomozygous60886334
1146968155146968159TATT----28GENIChomozygous60886335
1146968444146968445GA25GENIChomozygous60886336
1146969722146969723AAGCTAC21GENIChomozygous60886339
1146969843146969847CTCT----17GENIChomozygous60886340
1146969992146969993T-16GENIChomozygous60886341
1146970257146970258AAT16GENIChomozygous60886342
1146970691146970692CT24GENIChomozygous60886343
1146971220146971221GA30GENIChomozygous60886344
1146971401146971402GA23GENIChomozygous60886345
1146971549146971550GC32GENIChomozygous60886346