chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
94101757841017579TC36GENIChomozygous51926773
94101779041017791AG21GENIChomozygous51926775
94101786741017868TC19GENIChomozygous51926779
94101815041018151AG36GENIChomozygous51926783
94102136641021367GGTT19GENIChomozygous52381253
94102137441021376GG--19GENICheterozygous51926807
94102355841023559CA49GENICpossibly homozygous52381255
94102713641027137AAGT17GENICheterozygous51926841
94102762241027624TG--19GENICheterozygous52381261
94102766441027665AATGTG16GENIChomozygous51926856
94102798741027988AG34GENIChomozygous51926863
94103017341030175TG--14GENIChomozygous52381265
94103276441032765TG29GENICheterozygous51926901
94103357341033575TG--10GENICheterozygous52381267
94103449641034498TG--18GENIChomozygous51926915
94103773341037734G-24GENICheterozygous51926933
94104321541043217AT--32GENICpossibly homozygous52381275
94103035341030354AAGT7GENICheterozygous52543075