| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:196942039-196942174 | Common:2; Rare:40 | ||||
| chr3:196942301-196942695 | Common:2; Rare:171 | ||||
| chr3:197183852-197184161 | Rare:50 | ||||
| chr3:197736746-197737244 | Common:3; Rare:154 | ||||
| chr3:197749629-197750171 | Common:1; Rare:168 | ||||
| chr3:197791181-197791340 | Common:1; Rare:72 | ||||
| chr3:197949871-197950251 | Common:4; Rare:115; Clinvar (benign):2 | ||||
| chr3:197950657-197950978 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:197959926-197960264 | Common:1; Rare:115 | ||||
| chr4:53079-53387 | Rare:5 | ||||
| chr4:124324-124543 | Common:6; Rare:63 | ||||
| chr4:124982-125019 | Rare:11 | ||||
| chr4:337415-337918 | Common:6; Rare:142 | ||||
| chr4:474057-474357 | Common:3; Rare:104 | ||||
| chr4:499108-499350 | Common:3; Rare:103 |