| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:24795544-24795619 | Common:1; Rare:15 | ||||
| chr4:25160344-25160732 | Common:3; Rare:119; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233841-25234073 | Rare:97 | ||||
| chr4:25376979-25377344 | Common:3; Rare:111 | ||||
| chr4:25914036-25914308 | Common:2; Rare:117 | ||||
| chr4:26320420-26320859 | Common:1; Rare:146 | ||||
| chr4:26320868-26321057 | Rare:65; Clinvar (benign):1 | ||||
| chr4:26860565-26860812 | Common:2; Rare:81 | ||||
| chr4:36243822-36244020 | Common:1; Rare:41 | ||||
| chr4:37243888-37244191 | Common:4; Rare:66 | ||||
| chr4:37453830-37453982 | Rare:54 | ||||
| chr4:37826443-37826771 | Common:8; Rare:115 | ||||
| chr4:37977178-37977473 | Rare:72 | ||||
| chr4:38664248-38664315 | Rare:26 | ||||
| chr4:38867565-38867826 | Common:2; Rare:88 |