chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106567412565674126CG22GENIChomozygous116619195
106567467665674677TC4GENIChomozygous116619197
106567648865676489GT14GENIChomozygous116619199
106567853265678533CT21GENIChomozygous116619201
106567862065678621AC16GENIChomozygous116619203
106568031965680320GA21GENIChomozygous116619205
106568056965680570TC23GENIChomozygous116619207
106568157665681577TA13GENIChomozygous116619209
106568271865682719GC9GENIChomozygous126385185
106568272565682726TC7GENIChomozygous126385186
106568278765682788AT4GENICheterozygous116793185
106568355165683552GA22GENIChomozygous116619211
106568426665684267CT5GENIChomozygous117013651
106568525765685258GA15GENIChomozygous116619213
106568565365685654GA21GENIChomozygous116619215
106568674165686742AC4GENIChomozygous117172465
106568692365686924CT11GENIChomozygous116619217
106568704465687045GA26GENIChomozygous116619219
106568710065687101TC21GENIChomozygous116619221
106568733265687333CT15GENIChomozygous116619223
106568798965687990AC13GENIChomozygous116619225
106568969965689700AG4GENIChomozygous116619229
106568976465689765GA25GENIChomozygous116619231
106569002365690024TC25GENIChomozygous116619233
106569047065690471TA23GENIChomozygous116619235