| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:499124-499307 | Common:3; Rare:72 | ||||
| chr4:663592-663753 | Rare:54 | ||||
| chr4:673822-673949 | Common:1; Rare:50 | ||||
| chr4:674210-674596 | Common:4; Rare:180 | ||||
| chr4:681142-681235 | Rare:33 | ||||
| chr4:932264-932492 | Common:2; Rare:89 | ||||
| chr4:986894-987153 | Common:3; Rare:89; Clinvar:3; Clinvar (benign):2 | ||||
| chr4:1113524-1113632 | Common:2; Rare:39 | ||||
| chr4:1249988-1250023 | Common:1; Rare:6 | ||||
| chr4:2041875-2042068 | Common:1; Rare:74 | ||||
| chr4:2468820-2469210 | Common:5; Rare:162 | ||||
| chr4:2843710-2844022 | Common:3; Rare:109 | ||||
| chr4:2934773-2934894 | Common:1; Rare:58 | ||||
| chr4:3074431-3074692 | Common:5; Rare:81 | ||||
| chr4:3249048-3249281 | Rare:78 |