| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67401754-67402075 | Common:3; Rare:116 | ||||
| chr11:67428252-67428623 | Common:1; Rare:130 | ||||
| chr11:67428817-67429150 | Common:1; Rare:113 | ||||
| chr11:67432512-67432831 | Common:2; Rare:108 | ||||
| chr11:67443458-67443604 | Common:1; Rare:55 | ||||
| chr11:67468187-67468233 | Common:1; Rare:8 | ||||
| chr11:67482941-67483215 | Rare:67; Clinvar:2; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr11:67508090-67508239 | Common:1; Rare:46 | ||||
| chr11:68038941-68039064 | Rare:38; Clinvar:1 | ||||
| chr11:68213505-68213905 | Common:1; Rare:222 | ||||
| chr11:68271855-68272115 | Common:2; Rare:103 | ||||
| chr11:68460223-68460309 | Common:2; Rare:46 | ||||
| chr11:68841779-68841886 | Common:1; Rare:40; Clinvar (benign):3 | ||||
| chr11:68903774-68903943 | Common:4; Rare:80; Clinvar (benign):6 | ||||
| chr11:68929972-68930172 | Rare:42 |