| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:775253-775329 | Rare:21 | ||||
| chr4:778805-778845 | Rare:4 | ||||
| chr4:868627-868830 | Common:1; Rare:70 | ||||
| chr4:1001315-1001372 | Common:1; Rare:11 | ||||
| chr4:1167508-1167806 | Common:2; Rare:133 | ||||
| chr4:1177776-1177796 | Rare:2 | ||||
| chr4:1178693-1178745 | Rare:7 | ||||
| chr4:1202257-1202462 | Common:2; Rare:45 | ||||
| chr4:1345480-1345713 | Common:1; Rare:44 | ||||
| chr4:1806073-1806318 | Common:2; Rare:93; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):3 | ||||
| chr4:2747851-2748097 | Common:1; Rare:65 | ||||
| chr4:2931259-2931384 | Common:1; Rare:52 | ||||
| chr4:2935932-2936035 | Rare:15 | ||||
| chr4:3041522-3041824 | Common:4; Rare:75 | ||||
| chr4:3514752-3515097 | Common:4; Rare:134 |