| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:65570420-65570494 | Rare:34 | ||||
| chr11:65614186-65614230 | Rare:14 | ||||
| chr11:65614241-65614382 | Rare:25 | ||||
| chr11:65662890-65663006 | Common:1; Rare:33 | ||||
| chr11:65712158-65712288 | Rare:48 | ||||
| chr11:65860456-65860756 | Common:2; Rare:96 | ||||
| chr11:65872688-65872930 | Common:2; Rare:62; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:65888402-65888640 | Common:1; Rare:87 | ||||
| chr11:65900335-65900532 | Common:2; Rare:38 | ||||
| chr11:65961509-65961773 | Common:1; Rare:94 | ||||
| chr11:66002105-66002561 | Common:3; Rare:130; Clinvar:6; Clinvar (benign):3 | ||||
| chr11:66257618-66257819 | Rare:59 | ||||
| chr11:66268323-66268682 | Common:3; Rare:101 | ||||
| chr11:66288999-66289427 | Common:1; Rare:109 | ||||
| chr11:66345040-66345136 | Common:1; Rare:34 |