| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:151099477-151099713 | Common:3; Rare:93 | ||||
| chr4:151408888-151409267 | Common:4; Rare:121 | ||||
| chr4:152536054-152536389 | Common:2; Rare:126 | ||||
| chr4:152779721-152780176 | Common:2; Rare:116 | ||||
| chr4:153152951-153153147 | Rare:38 | ||||
| chr4:154491776-154492006 | Common:1; Rare:49 | ||||
| chr4:156970570-156970658 | Rare:18 | ||||
| chr4:156970933-156971199 | Rare:41 | ||||
| chr4:157076004-157076250 | Common:1; Rare:74; Clinvar (benign):2 | ||||
| chr4:158173023-158173172 | Rare:24 | ||||
| chr4:158671825-158672365 | Common:5; Rare:136; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:158723319-158723463 | Common:2; Rare:66 | ||||
| chr4:158805634-158805850 | Common:1; Rare:36 | ||||
| chr4:163166829-163166957 | Common:2; Rare:40 | ||||
| chr4:163332587-163332611 | Rare:4 |