| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196712199-196712344 | Common:2; Rare:49 | ||||
| chr3:196942363-196942650 | Common:1; Rare:118 | ||||
| chr3:197736854-197737148 | Common:3; Rare:93 | ||||
| chr3:197749830-197749984 | Rare:66 | ||||
| chr3:197791069-197791281 | Common:3; Rare:68 | ||||
| chr3:197949875-197950259 | Common:4; Rare:113; Clinvar (benign):2 | ||||
| chr3:197959968-197960245 | Common:1; Rare:97 | ||||
| chr4:124314-124520 | Common:6; Rare:52 | ||||
| chr4:337632-337849 | Rare:58 | ||||
| chr4:499140-499297 | Common:3; Rare:57 | ||||
| chr4:674210-674558 | Common:2; Rare:160 | ||||
| chr4:932250-932487 | Common:2; Rare:93 | ||||
| chr4:1171161-1171362 | Common:2; Rare:90 | ||||
| chr4:1201521-1201626 | Rare:30 | ||||
| chr4:1289650-1289916 | Common:1; Rare:89 |