| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr5:154857855-154857889 | Rare:8 | ||||
| chr5:154857927-154858252 | Common:6; Rare:103 | ||||
| chr5:154858475-154858722 | Common:1; Rare:78 | ||||
| chr5:154938156-154938286 | Rare:47 | ||||
| chr5:154941003-154941257 | Common:1; Rare:106 | ||||
| chr5:156326936-156327228 | Common:2; Rare:67; Clinvar:3; Clinvar (benign):3 | ||||
| chr5:157143610-157143721 | Rare:27 | ||||
| chr5:157266009-157266188 | Common:1; Rare:50 | ||||
| chr5:157266694-157266799 | Rare:17 | ||||
| chr5:157575130-157575263 | Rare:30 | ||||
| chr5:157731379-157731462 | Common:3; Rare:36 | ||||
| chr5:159097563-159097802 | Common:1; Rare:47 | ||||
| chr5:159099778-159099865 | Common:3; Rare:7 | ||||
| chr5:159208084-159208206 | Common:2; Rare:21 | ||||
| chr5:159263191-159263330 | Common:1; Rare:44 |