| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:152936225-152936402 | Common:3; Rare:49 | ||||
| chr4:152936751-152936999 | Common:1; Rare:55 | ||||
| chr4:153257186-153257591 | Common:2; Rare:70 | ||||
| chr4:153344510-153344784 | Common:4; Rare:97 | ||||
| chr4:153759386-153759643 | Rare:48 | ||||
| chr4:153759864-153759964 | Rare:16 | ||||
| chr4:153759972-153760082 | Common:2; Rare:30 | ||||
| chr4:153760155-153760291 | Common:2; Rare:31 | ||||
| chr4:153788862-153789233 | Rare:104 | ||||
| chr4:154550304-154550523 | Common:2; Rare:72 | ||||
| chr4:155352915-155353301 | Common:1; Rare:98 | ||||
| chr4:158671797-158672427 | Common:5; Rare:173; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:158723206-158723463 | Common:2; Rare:110 | ||||
| chr4:158768853-158769027 | Common:1; Rare:59 | ||||
| chr4:162163991-162164130 | Common:1; Rare:35 |