| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:236913-237062 | Common:1; Rare:58 | ||||
| chr11:289014-289185 | Common:1; Rare:48 | ||||
| chr11:506676-507007 | Common:3; Rare:104 | ||||
| chr11:507140-507534 | Common:4; Rare:131 | ||||
| chr11:560701-561003 | Common:6; Rare:141 | ||||
| chr11:576412-576519 | Rare:43 | ||||
| chr11:747306-747526 | Rare:89; Clinvar:2; Clinvar (benign):1 | ||||
| chr11:763341-763943 | Rare:263; Clinvar:5; Clinvar (pathogenic):3 | ||||
| chr11:777463-777623 | Common:1; Rare:69 | ||||
| chr11:797950-798025 | Rare:22 | ||||
| chr11:809486-810037 | Common:5; Rare:206 | ||||
| chr11:832833-833018 | Common:7; Rare:62 | ||||
| chr11:842435-842984 | Common:8; Rare:224 | ||||
| chr11:843964-844165 | Common:1; Rare:48 | ||||
| chr11:1309563-1309836 | Common:1; Rare:115 |