| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:153789067-153789222 | Rare:30 | ||||
| chr4:154743848-154744013 | Rare:65 | ||||
| chr4:156970880-156971229 | Common:1; Rare:61 | ||||
| chr4:156971734-156972080 | Common:3; Rare:123 | ||||
| chr4:158172369-158172435 | Rare:13 | ||||
| chr4:158172986-158173090 | Rare:20 | ||||
| chr4:158210132-158210567 | Common:4; Rare:98 | ||||
| chr4:158671825-158672171 | Common:4; Rare:94; Clinvar:1 | ||||
| chr4:158672208-158672457 | Common:1; Rare:67; Clinvar:2; Clinvar (benign):2 | ||||
| chr4:158723311-158723463 | Common:2; Rare:69 | ||||
| chr4:159103823-159104175 | Common:4; Rare:125 | ||||
| chr4:159228261-159228328 | Rare:9 | ||||
| chr4:163166261-163166459 | Common:1; Rare:76 | ||||
| chr4:163166832-163166957 | Common:2; Rare:40 | ||||
| chr4:163332544-163332669 | Common:1; Rare:18 |