| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:10856429-10856829 | Common:8; Rare:144 | ||||
| chr4:11223328-11223573 | Rare:66 | ||||
| chr4:13483201-13483383 | Common:1; Rare:49 | ||||
| chr4:13484956-13485356 | Common:3; Rare:104 | ||||
| chr4:13531375-13531775 | Common:1; Rare:114 | ||||
| chr4:13544139-13544361 | Common:1; Rare:97; Clinvar:3; Clinvar (benign):1 | ||||
| chr4:13547097-13547702 | Common:10; Rare:316 | ||||
| chr4:13640210-13640630 | Common:1; Rare:69 | ||||
| chr4:13654237-13654340 | Rare:24 | ||||
| chr4:13654510-13654870 | Rare:74 | ||||
| chr4:13784049-13784449 | Common:4; Rare:100 | ||||
| chr4:15001269-15001507 | Common:1; Rare:52 | ||||
| chr4:15118210-15118610 | Rare:210 | ||||
| chr4:15144304-15144704 | Common:2; Rare:109 | ||||
| chr4:15653880-15654210 | Common:5; Rare:70 |