chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
106566568965665690CT43GENIChomozygous116793169
106566668865666689TC26GENIChomozygous116793171
106566960465669605AG36GENIChomozygous116793173
106567053265670533GC58GENICheterozygous118041708
106567054865670549GA55GENICheterozygous118041709
106567055065670551GA55GENICheterozygous118041710
106567057965670580TA44GENICheterozygous118041711
106567411865674119GA31GENIChomozygous116793175
106567643265676433CT50GENICpossibly homozygous116793177
106567859565678596GA42GENICpossibly homozygous116793179
106567877365678774AG28GENIChomozygous116793181
106567900465679005GT35GENIChomozygous116793183
106567412565674126CG29GENIChomozygous116619195
106567467665674677TC46GENIChomozygous116619197
106567648865676489GT51GENIChomozygous116619199
106567862065678621AC44GENIChomozygous116619203
106567519365675194GC46GENICheterozygous118084166
106568278765682788AT12GENICpossibly homozygous116793185
106568279465682795GA11GENICpossibly homozygous116793187
106568298765682988CT38GENICpossibly homozygous116793189
106568355165683552GA37GENIChomozygous116619211
106568387665683877GA36GENIChomozygous116793191
106568506765685068GA33GENIChomozygous116793193
106568514465685145CA23GENIChomozygous116793195
106568565365685654GA30GENIChomozygous116619215
106568597865685979CT30GENIChomozygous116793197
106568683765686838CT22GENIChomozygous116793199
106568692365686924CT27GENIChomozygous116619217
106568710065687101TC38GENIChomozygous116619221
106568733265687333CT30GENIChomozygous116619223
106568798965687990AC25GENIChomozygous116619225
106568806965688070CT32GENICpossibly homozygous116793201
106568896265688963CA19GENIChomozygous116793203
106568969665689697CT31GENIChomozygous116619227
106568969965689700AG33GENIChomozygous116619229
106568973565689736GT33GENIChomozygous116793205
106569047065690471TA30GENIChomozygous116619235
106568603665686037TC37GENIChomozygous117130927
106568674165686742AC19GENICheterozygous117172465