| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151015220-151015407 | Rare:51 | ||||
| chr4:151099396-151099713 | Common:3; Rare:114 | ||||
| chr4:151100275-151100584 | Common:1; Rare:62 | ||||
| chr4:151408885-151409273 | Common:5; Rare:122 | ||||
| chr4:152536054-152536305 | Rare:100 | ||||
| chr4:152779721-152780021 | Common:1; Rare:84 | ||||
| chr4:153789081-153789188 | Rare:18 | ||||
| chr4:156970911-156971215 | Rare:50 | ||||
| chr4:158172360-158172678 | Rare:49 | ||||
| chr4:158172986-158173005 | Rare:4 | ||||
| chr4:158173012-158173115 | Rare:19 | ||||
| chr4:158671849-158672422 | Common:5; Rare:149; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:163166847-163166977 | Common:2; Rare:41 | ||||
| chr4:165327408-165327741 | Common:2; Rare:95 | ||||
| chr4:165873467-165873754 | Common:2; Rare:58 |