| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:46846218-46846414 | Common:1; Rare:54 | ||||
| chr11:47176807-47177138 | Common:1; Rare:143 | ||||
| chr11:47214837-47215110 | Common:2; Rare:69; Clinvar:3; Clinvar (benign):1 | ||||
| chr11:47269083-47269388 | Common:1; Rare:62 | ||||
| chr11:47270012-47270166 | Common:1; Rare:52 | ||||
| chr11:47553083-47553356 | Common:2; Rare:93 | ||||
| chr11:47565478-47565628 | Common:3; Rare:29 | ||||
| chr11:47578947-47579094 | Rare:76; Clinvar:2; Clinvar (pathogenic):1 | ||||
| chr11:47642452-47642728 | Rare:109 | ||||
| chr11:47848322-47848653 | Common:3; Rare:113 | ||||
| chr11:57311450-57311724 | Common:1; Rare:71 | ||||
| chr11:57324883-57325169 | Common:1; Rare:95 | ||||
| chr11:57514819-57515105 | Common:2; Rare:54 | ||||
| chr11:57530682-57530857 | Common:1; Rare:43 | ||||
| chr11:57657440-57657794 | Common:4; Rare:91 |