chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
158475085384750854GA29GENIChomozygous112746765
158475158584751586GA26GENIChomozygous112746767
158475407784754078CT20GENIChomozygous112746769
158475550784755508TA15GENIChomozygous112746771
158475717484757175TC16GENIChomozygous112746773
158475931284759313TG22GENIChomozygous112944204
158475960184759602GT32GENIChomozygous112746777
158475964084759641TC37GENIChomozygous112746779
158476002084760021GA40GENIChomozygous112746781
158476068484760685AG21GENIChomozygous112746783
158476094284760943CT11GENIChomozygous112746785
158476202684762027AC26GENIChomozygous112746787
158476876384768764AG30GENIChomozygous112746791
158476996284769963AG18GENIChomozygous112944206
158477260484772605AT51GENIChomozygous112944208
158477340784773408TC34GENIChomozygous112746799
158477468184774682CT30GENIChomozygous112746805
158477563784775638CT37GENIChomozygous112746809
158477629784776298GC64GENIChomozygous112944210
158477642984776430TC29GENIChomozygous112746811
158476150384761504CT8GENIChomozygous113203376
158476308084763081GA15GENIChomozygous112822352
158476558384765584CA30GENIChomozygous112822354
158476561184765612AG30GENIChomozygous112822356
158477715884777159GA14GENIChomozygous112944212
158477939384779394CT22GENIChomozygous112944214
158478447984784480GA28GENIChomozygous113203378
158478459884784599CT15GENIChomozygous112746821
158478461484784615AG19GENIChomozygous112944216