chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
3140107794140107795CA17GENIChomozygous111752222
3140108166140108167TC34GENIChomozygous111752224
3140108369140108370CT18GENIChomozygous111752228
3140108405140108406TG20GENIChomozygous112166913
3140108992140108993CT34GENIChomozygous112166915
3140109707140109708CT13GENIChomozygous112166919
3140112195140112196AT24GENIChomozygous112166921
3140112918140112919AG30GENIChomozygous111752236
3140113216140113217GA38GENIChomozygous112166923
3140113544140113545GA19GENIChomozygous111752239
3140114039140114040AG27GENIChomozygous111752243
3140114246140114247TC22GENIChomozygous111752244
3140114744140114745TC17GENIChomozygous111752246
3140117248140117249GT22GENIChomozygous111752250
3140119408140119409AG23GENIChomozygous111752256
3140119679140119680GA28GENIChomozygous111752258
3140119896140119897TC21GENIChomozygous111752262
3140120418140120419CT18GENIChomozygous112166925
3140120856140120857CT31GENIChomozygous112166927
3140121166140121167AG25GENICpossibly homozygous111752264
3140123197140123198GC31GENIChomozygous112166929
3140123851140123852CT18GENIChomozygous111752266