| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:4582899-4583033 | Common:2; Rare:22 | ||||
| chr4:4585572-4585628 | Common:1; Rare:10 | ||||
| chr4:4611596-4611666 | Common:2; Rare:15 | ||||
| chr4:4844056-4844228 | Common:3; Rare:46 | ||||
| chr4:4920687-4920816 | Rare:22 | ||||
| chr4:4923312-4923561 | Common:1; Rare:38 | ||||
| chr4:5436252-5436401 | Common:1; Rare:36 | ||||
| chr4:5653178-5653350 | Rare:32 | ||||
| chr4:6287013-6287187 | Rare:39; Clinvar (benign):2 | ||||
| chr4:6308636-6308827 | Common:2; Rare:63 | ||||
| chr4:6401580-6401725 | Rare:29 | ||||
| chr4:6673185-6673449 | Common:3; Rare:61 | ||||
| chr4:6673815-6673948 | Common:6; Rare:66 | ||||
| chr4:6688260-6688457 | Common:3; Rare:43 | ||||
| chr4:6709264-6709284 | Rare:5 |