chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
5160394685160394686GA9GENICpossibly homozygous114074195
5160394781160394782TC16GENIChomozygous114074196
5160394935160394936CT8GENIChomozygous118858976
5160394940160394941CA8GENIChomozygous118858977
5160394948160394949TC8GENIChomozygous114160900
5160395013160395014CT12GENIChomozygous114074198
5160395804160395805CT50GENIChomozygous114074199
5160396506160396507AC24GENIChomozygous114074207
5160396961160396962TC26GENIChomozygous114074209
5160397071160397072GA23GENIChomozygous114074210
5160398250160398251AG19GENIChomozygous114074211
5160401873160401874AG10GENIChomozygous114074217