| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:155208434-155208891 | Rare:92 | ||||
| chr4:155376771-155377040 | Rare:68 | ||||
| chr4:155758769-155759129 | Common:1; Rare:94 | ||||
| chr4:158671809-158672453 | Common:5; Rare:174; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723323-158723501 | Common:2; Rare:79 | ||||
| chr4:158805729-158805845 | Common:1; Rare:19 | ||||
| chr4:163166832-163166946 | Common:2; Rare:37 | ||||
| chr4:163494463-163494796 | Common:3; Rare:132 | ||||
| chr4:164956917-164957025 | Common:2; Rare:34 | ||||
| chr4:165112819-165113022 | Common:1; Rare:58 | ||||
| chr4:165327408-165327764 | Common:2; Rare:103 | ||||
| chr4:167234506-167234719 | Rare:56 | ||||
| chr4:168831907-168832092 | Common:2; Rare:50 | ||||
| chr4:169010223-169010474 | Common:1; Rare:80 | ||||
| chr4:169612538-169612797 | Common:5; Rare:85; Clinvar:4; Clinvar (benign):2 |