| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:197749832-197749968 | Rare:60 | ||||
| chr3:197791181-197791274 | Rare:36 | ||||
| chr3:197949871-197950288 | Common:4; Rare:123; Clinvar (benign):2 | ||||
| chr3:197959969-197960237 | Common:1; Rare:93 | ||||
| chr4:499149-499301 | Common:2; Rare:54 | ||||
| chr4:673842-673948 | Rare:45 | ||||
| chr4:674242-674533 | Rare:134 | ||||
| chr4:932250-932487 | Common:2; Rare:93 | ||||
| chr4:1289650-1289919 | Common:1; Rare:91 | ||||
| chr4:2468820-2469167 | Common:4; Rare:132 | ||||
| chr4:2934787-2934928 | Common:4; Rare:67 | ||||
| chr4:4248147-4248260 | Common:4; Rare:59 | ||||
| chr4:4290080-4290235 | Common:3; Rare:64 | ||||
| chr4:4541970-4542208 | Common:2; Rare:97 | ||||
| chr4:6640537-6640716 | Common:2; Rare:74 |