| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:932162-932492 | Common:2; Rare:125 | ||||
| chr4:1113497-1113620 | Common:2; Rare:48 | ||||
| chr4:1172800-1173113 | Common:5; Rare:43 | ||||
| chr4:1346792-1347211 | Common:6; Rare:123 | ||||
| chr4:1720362-1720596 | Common:2; Rare:63 | ||||
| chr4:2468878-2469178 | Common:4; Rare:116 | ||||
| chr4:2843689-2843970 | Common:3; Rare:100 | ||||
| chr4:2934779-2934942 | Common:4; Rare:77 | ||||
| chr4:2963332-2963611 | Common:2; Rare:99 | ||||
| chr4:3532211-3532264 | Rare:18; Clinvar (pathogenic):2 | ||||
| chr4:4248189-4248266 | Common:2; Rare:35 | ||||
| chr4:4290117-4290304 | Common:3; Rare:74 | ||||
| chr4:4541934-4542143 | Common:1; Rare:84 | ||||
| chr4:6575064-6575214 | Common:2; Rare:52 | ||||
| chr4:6640518-6640898 | Common:3; Rare:130 |