| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197736694-197737221 | Common:3; Rare:168 | ||||
| chr3:197749332-197749492 | Common:1; Rare:36 | ||||
| chr3:197749830-197749972 | Rare:63 | ||||
| chr3:197791068-197791281 | Common:3; Rare:68 | ||||
| chr3:197949893-197950250 | Common:4; Rare:111; Clinvar (benign):2 | ||||
| chr3:197959969-197960237 | Common:1; Rare:93 | ||||
| chr4:337632-337920 | Common:4; Rare:82 | ||||
| chr4:499141-499281 | Common:2; Rare:46 | ||||
| chr4:674248-674599 | Common:3; Rare:166 | ||||
| chr4:932300-932487 | Common:2; Rare:76 | ||||
| chr4:1289659-1289906 | Common:1; Rare:79 | ||||
| chr4:2041945-2042028 | Rare:40 | ||||
| chr4:2468878-2469187 | Common:4; Rare:122 | ||||
| chr4:2812193-2812300 | Rare:17 | ||||
| chr4:2843667-2843951 | Common:1; Rare:104 |