| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:95067014-95067258 | Rare:74 | ||||
| chr11:95067398-95067968 | Common:3; Rare:229 | ||||
| chr11:95089444-95089961 | Common:7; Rare:162 | ||||
| chr11:95231168-95231671 | Common:3; Rare:151 | ||||
| chr11:95232296-95232527 | Rare:44 | ||||
| chr11:95788788-95789142 | Common:1; Rare:111 | ||||
| chr11:95789420-95789550 | Common:1; Rare:58 | ||||
| chr11:95789716-95790259 | Common:4; Rare:183 | ||||
| chr11:95790319-95790714 | Common:3; Rare:156 | ||||
| chr11:95791006-95791243 | Rare:83 | ||||
| chr11:95923766-95923905 | Common:1; Rare:55; Clinvar:2; Clinvar (benign):3 | ||||
| chr11:95923906-95924264 | Common:1; Rare:140; Clinvar:4; Clinvar (benign):2 | ||||
| chr11:96343291-96343581 | Common:1; Rare:65 | ||||
| chr11:96389312-96389430 | Common:1; Rare:29 | ||||
| chr11:96389610-96389658 | Common:1; Rare:13 |