| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196639623-196639789 | Rare:38 | ||||
| chr3:196712216-196712344 | Common:2; Rare:42 | ||||
| chr3:196942399-196942670 | Common:1; Rare:110 | ||||
| chr3:197298577-197298751 | Rare:56 | ||||
| chr3:197749722-197749978 | Common:1; Rare:94 | ||||
| chr3:197949894-197950250 | Common:4; Rare:110; Clinvar (benign):2 | ||||
| chr3:197959968-197960242 | Common:1; Rare:97 | ||||
| chr4:499123-499333 | Common:3; Rare:85 | ||||
| chr4:674248-674552 | Common:1; Rare:142 | ||||
| chr4:932181-932487 | Common:2; Rare:119 | ||||
| chr4:1113533-1113604 | Common:1; Rare:27 | ||||
| chr4:1289665-1289916 | Common:1; Rare:80 | ||||
| chr4:2468878-2469184 | Common:4; Rare:119 | ||||
| chr4:2934779-2934906 | Common:1; Rare:61 | ||||
| chr4:2963353-2963587 | Common:1; Rare:75 |