chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
154126701341267014G32GENIChomozygous129249214
154126704441267045C31GENIChomozygous129249215
154126705141267052C31GENIChomozygous129249216
154126708841267089C24GENIChomozygous129249217
154126710441267104TTA24GENIChomozygous129249218
154127160641271606G30GENIChomozygous129249219
154127161741271617A30GENICpossibly homozygous129249220
154127172141271722C35GENIChomozygous129249221
154127177341271774C36GENIChomozygous129249222
154128629941286300T10GENIChomozygous129249223
154128636941286369G29GENIChomozygous129249224
154128638841286388G23GENIChomozygous129249225
154128642241286422CT15GENIChomozygous129249226
154128642441286425G13GENIChomozygous129249227
154128645941286460G11GENIChomozygous129249228
154128647141286472T7GENIChomozygous129249229
154128649541286495T9GENIChomozygous129249230
154128650341286504TG8GENIChomozygous129315315
154128650541286520TTTTTTTTTTTTTAG8GENIChomozygous129249231
154128652241286528TCAAAA10GENIChomozygous129249232
154128653641286536G13GENIChomozygous129249233
154128657341286574G23GENIChomozygous129249234
154128663541286636T42GENIChomozygous129249235
154128666241286663T45GENIChomozygous129249236
154128667341286674G46GENIChomozygous129249237
154127161341271614TG28GENIChomozygous112914233
154131307041313070A8GENIChomozygous130440670