| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197949890-197950235 | Common:4; Rare:106; Clinvar (benign):1 | ||||
| chr3:197959989-197960244 | Common:1; Rare:90 | ||||
| chr4:499141-499289 | Common:2; Rare:50 | ||||
| chr4:673302-673608 | Rare:117 | ||||
| chr4:674212-674605 | Common:4; Rare:182 | ||||
| chr4:689141-689302 | Common:3; Rare:41 | ||||
| chr4:705578-705851 | Rare:89 | ||||
| chr4:932264-932487 | Common:2; Rare:87 | ||||
| chr4:986919-987035 | Common:1; Rare:30; Clinvar:1 | ||||
| chr4:1113517-1113632 | Common:2; Rare:40 | ||||
| chr4:1309403-1309645 | Common:3; Rare:65 | ||||
| chr4:2041912-2042068 | Common:1; Rare:61 | ||||
| chr4:2468878-2469155 | Common:3; Rare:98 | ||||
| chr4:2843721-2844009 | Common:3; Rare:99 | ||||
| chr4:2934771-2934917 | Common:3; Rare:69 |