chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
X1536010115360102GT9INTERGENIChomozygous62914165
X1536036715360368AC16INTERGENIChomozygous62914166
X1536043815360439AC18INTERGENIChomozygous62914167
X1536209215362093CT8INTERGENICheterozygous62914169
X1536594515365946AG6INTERGENIChomozygous62914170
X1536876415368765AC16INTERGENIChomozygous62914171
X1537431815374319AG9INTERGENIChomozygous62914172
X1537743915377440AC7INTERGENIChomozygous62914173
X1537797315377974CG5INTERGENIChomozygous62914174
X1538145115381452GC2INTERGENIChomozygous62914177
X1538153415381535CT11INTERGENIChomozygous62914178
X1538250015382501GC2INTERGENICheterozygous62914179
X1538250115382502GA2INTERGENICheterozygous62914180
X1538251915382520CT1INTERGENIChomozygous62914182
X1538571815385719CG11INTERGENIChomozygous62914192
X1538700415387005AC2INTERGENIChomozygous62914193
X1538744315387444AT9INTERGENIChomozygous62914194
X1538790915387910AG8INTERGENICpossibly homozygous62914195
X1538912515389126CT13INTERGENIChomozygous62914196
X1539102315391024CT8INTERGENIChomozygous62914197