chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
41130571111305712TC21GENIChomozygous136971001
41130669411306695AC26GENIChomozygous136971002
41130733011307331TC22GENIChomozygous136971003
41130753911307540GA19GENIChomozygous136971004
41130771711307718CG20GENIChomozygous136971005
41130799011307991AG16GENIChomozygous136971006
41130828611308287GA29GENIChomozygous136971007
41131010611310107GT16GENIChomozygous136971008
41131100411311005TC29GENIChomozygous136971009
41131156011311561TC24GENIChomozygous136971010
41131162611311627TG23GENICpossibly homozygous136971011
41130857911308581TG21GENIChomozygous136866704
41131142111311422T17GENICpossibly homozygous136866705
41131144511311445T18GENIChomozygous136866706