| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:67428303-67428632 | Common:1; Rare:308 | ||||
| chr11:67443398-67443837 | Common:6; Rare:290 | ||||
| chr11:67464593-67465000 | Rare:475 | ||||
| chr11:67468179-67468282 | Common:1; Rare:19 | ||||
| chr11:67469114-67469472 | Common:10; Rare:335 | ||||
| chr11:67482836-67483237 | Common:1; Rare:232; Clinvar:7; Clinvar (benign):12; Clinvar (pathogenic):6 | ||||
| chr11:67489223-67490197 | Common:12; Rare:393; Clinvar:10; Clinvar (benign):11; Clinvar (pathogenic):7 | ||||
| chr11:67502470-67502810 | Rare:91 | ||||
| chr11:67505292-67505492 | Rare:77 | ||||
| chr11:67506100-67506220 | Common:1; Rare:27 | ||||
| chr11:67507720-67507955 | Rare:114 | ||||
| chr11:67508015-67508546 | Common:3; Rare:330 | ||||
| chr11:67508596-67508786 | Common:8; Rare:158 | ||||
| chr11:67607960-67608613 | Common:3; Rare:183; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):3 | ||||
| chr11:67629240-67629560 | Common:1; Rare:99 |