| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197949885-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959989-197960245 | Common:1; Rare:90 | ||||
| chr4:499136-499289 | Common:3; Rare:53 | ||||
| chr4:673840-673960 | Rare:49 | ||||
| chr4:674234-674573 | Common:2; Rare:158 | ||||
| chr4:932259-932492 | Common:2; Rare:90 | ||||
| chr4:1113537-1113627 | Common:1; Rare:34 | ||||
| chr4:1289670-1289906 | Common:1; Rare:75 | ||||
| chr4:2468846-2469167 | Common:4; Rare:119 | ||||
| chr4:2843696-2844013 | Common:3; Rare:117 | ||||
| chr4:2934779-2934894 | Common:1; Rare:55 | ||||
| chr4:4248198-4248276 | Common:1; Rare:32 | ||||
| chr4:4290110-4290291 | Common:3; Rare:73 | ||||
| chr4:4541976-4542143 | Common:1; Rare:67 | ||||
| chr4:6640528-6640726 | Common:3; Rare:83 |