chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151256925412569255GA13GENIChomozygous112452423
151256930912569310CT13GENIChomozygous112985219
151257142412571425TA21GENIChomozygous112985220
151257290012572900T20GENIChomozygous132900380
151257470612574707TC20GENIChomozygous112452427
151257505812575058T10GENIChomozygous132900381
151257517512575176AC11GENIChomozygous112985221
151256936712569367C12GENIChomozygous129230626
151257100212571004TC20GENIChomozygous129230627
151257402712574028A18GENIChomozygous129230628
151257634412576345AG5GENIChomozygous112452428
151257641912576420TC14GENIChomozygous112452430
151257739112577392GA9GENIChomozygous112452432
151257978412579785GT21GENIChomozygous112452435
151258022912580230AG20GENIChomozygous112452436
151258127912581280CG19GENIChomozygous112985222
151257442612574427AG15GENIChomozygous118870228
151257562512575632TTATTAT13GENIChomozygous129230631
151257524112575241TGAGCTGACTTACAGCTG8GENIChomozygous129230629
151257526012575261T12GENIChomozygous129230630
151257737012577372TA12GENIChomozygous132900382
151258059512580596T24GENIChomozygous132900383
151258125012581252AT20GENIChomozygous132900384
151258386212583864GT24GENIChomozygous129230635
151258200012582001TG20GENIChomozygous112900352
151258339212583393AG29GENIChomozygous112452440
151257738912577390GA9GENIChomozygous132903640
151258092012580920C10GENIChomozygous134026555
151257735512577357AT11GENIChomozygous131517772