chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
151256925412569255GA14GENIChomozygous112452423
151256930912569310CT15GENIChomozygous112985219
151257142412571425TA35GENIChomozygous112985220
151257470612574707TC13GENIChomozygous112452427
151256936712569367C7GENIChomozygous129230626
151257100212571004TC29GENIChomozygous129230627
151257402712574028A20GENIChomozygous129230628
151256959912569600GC7GENICpossibly homozygous113161685
151257290012572900T24GENIChomozygous132900380
151257442612574427AG15GENIChomozygous118870228
151257505812575058T13GENICpossibly homozygous132900381
151257517512575176AC6GENIChomozygous112985221
151257524112575241TGAGCTGACTTACAGCTG5GENIChomozygous129230629
151257526012575261T8GENIChomozygous129230630
151257562512575632TTATTAT17GENIChomozygous129230631
151257634412576345AG10GENIChomozygous112452428
151257641912576420TC17GENIChomozygous112452430
151257735512577357AT10GENIChomozygous131517772
151257737012577372TA11GENIChomozygous132900382
151257739112577392GA10GENIChomozygous112452432
151257978412579785GT17GENIChomozygous112452435
151258022912580230AG24GENIChomozygous112452436
151258059512580596T21GENIChomozygous132900383
151258125012581252AT26GENIChomozygous132900384
151258127912581280CG23GENIChomozygous112985222
151258339212583393AG24GENIChomozygous112452440
151258386212583864GT16GENIChomozygous129230635
151257738912577390GA10GENIChomozygous132903640
151258200012582001TG17GENIChomozygous112900352
151258092012580920C8GENIChomozygous134026555