chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41130571111305712TC40GENIChomozygous136971001
41130669411306695AC51GENIChomozygous136971002
41130733011307331TC53GENIChomozygous136971003
41130753911307540GA37GENIChomozygous136971004
41130771711307718CG56GENIChomozygous136971005
41130799011307991AG43GENIChomozygous136971006
41130828611308287GA48GENIChomozygous136971007
41131010611310107GT39GENIChomozygous136971008
41131100411311005TC50GENIChomozygous136971009
41131144511311445T36GENIChomozygous136866706
41130857911308581TG35GENIChomozygous136866704
41131142111311422T31GENICpossibly homozygous136866705
41131050811310520CTTTCTTTCTTC6GENIChomozygous140874123
41131057111310572TC20GENICheterozygous140877699
41131057211310573CT19GENICheterozygous140877700
41131057911310580TC21GENICheterozygous140877701
41131156011311561TC48GENIChomozygous136971010
41131162611311627TG41GENICpossibly homozygous136971011
41131059511310596TC25GENICheterozygous403955348
41131059511310596T25GENICheterozygous403955349