chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3140107794140107795CA18GENIChomozygous111752222
3140108166140108167TC31GENIChomozygous111752224
3140108369140108370CT37GENIChomozygous111752228
3140108992140108993CT24GENIChomozygous112166915
3140109175140109176GA12GENIChomozygous112166917
3140109707140109708CT16GENIChomozygous112166919
3140112195140112196AT22GENIChomozygous112166921
3140112918140112919AG24GENIChomozygous111752236
3140113216140113217GA21GENIChomozygous112166923
3140113544140113545GA22GENICpossibly homozygous111752239
3140114039140114040AG34GENIChomozygous111752243
3140114246140114247TC17GENIChomozygous111752244
3140114744140114745TC5GENIChomozygous111752246
3140117248140117249GT6GENIChomozygous111752250
3140119408140119409AG19GENIChomozygous111752256
3140119679140119680GA20GENIChomozygous111752258
3140119896140119897TC9GENIChomozygous111752262
3140120418140120419CT6GENIChomozygous112166925
3140120856140120857CT13GENIChomozygous112166927
3140121166140121167AG18GENIChomozygous111752264
3140123197140123198GC25GENIChomozygous112166929
3140123851140123852CT12GENIChomozygous111752266