chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
114547756045477561AT11GENIChomozygous115963452
114547769945477700TC19GENIChomozygous115854161
114547812745478128CT33GENIChomozygous115854163
114547859145478592CT31GENIChomozygous115854165
114547943845479439AG33GENIChomozygous115854169
114547947745479478TC34GENIChomozygous115854171
114547952745479528GC16GENIChomozygous115854173
114548183445481835GA20GENIChomozygous115854177
114548237745482378TC9GENIChomozygous115854179
114548282245482823GC27GENIChomozygous116186049
114548321445483215AC21GENIChomozygous115854181
114548419545484196CA21GENIChomozygous115854185
114548483545484836GT11GENIChomozygous116186051
114548483945484840AG11GENIChomozygous116186053
114548492145484922GT6GENIChomozygous116186055
114548746245487463CG23GENIChomozygous115854187
114548752045487521AT33GENIChomozygous116186057
114548771645487717TC17GENIChomozygous116186059
114548776745487768AG13GENIChomozygous115854189
114548989745489898AG30GENIChomozygous115854191
114549067145490672AC18GENIChomozygous115854195
114549201645492017AG24GENIChomozygous115854197
114549220345492204AC5GENIChomozygous116186061
114549321645493217TG22GENIChomozygous115963454
114549703245497033AC20GENIChomozygous116186063
114550461945504620TC22GENIChomozygous115854205
114550874445508745AG17GENIChomozygous116186065
114550909645509097TG18GENIChomozygous116186067
114550985045509851GA33GENIChomozygous115854211
114551120345511204AG21GENIChomozygous115854213