| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr4:15655232-15655482 | Common:2; Rare:101 | ||||
| chr4:15681478-15681893 | Common:4; Rare:146 | ||||
| chr4:16898497-16898876 | Common:14; Rare:71 | ||||
| chr4:17577316-17577539 | Rare:106 | ||||
| chr4:17614551-17614660 | Common:2; Rare:48 | ||||
| chr4:17810514-17811056 | Common:4; Rare:159 | ||||
| chr4:18021608-18021920 | Common:2; Rare:146 | ||||
| chr4:20252867-20252928 | Rare:18 | ||||
| chr4:20253262-20253493 | Common:2; Rare:53 | ||||
| chr4:20700217-20700499 | Common:1; Rare:120 | ||||
| chr4:23890016-23890264 | Common:1; Rare:40 | ||||
| chr4:24584198-24584245 | Rare:20 | ||||
| chr4:25160340-25160692 | Common:3; Rare:109; Clinvar:2; Clinvar (benign):1 | ||||
| chr4:25233837-25234050 | Rare:91 | ||||
| chr4:25376966-25377325 | Common:4; Rare:107 |