| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:35556969-35557249 | Common:2; Rare:87 | ||||
| chr20:35616792-35617026 | Common:1; Rare:45 | ||||
| chr20:35664770-35665005 | Common:1; Rare:65 | ||||
| chr20:35699107-35699264 | Rare:28 | ||||
| chr20:35699295-35699493 | Rare:69; Clinvar (benign):3 | ||||
| chr20:35740801-35741126 | Common:3; Rare:94 | ||||
| chr20:35741618-35741685 | Common:1; Rare:22 | ||||
| chr20:35741939-35742675 | Common:7; Rare:246 | ||||
| chr20:35771784-35772077 | Common:2; Rare:89 | ||||
| chr20:36236454-36236503 | Rare:12 | ||||
| chr20:36461133-36461498 | Common:1; Rare:107 | ||||
| chr20:36472984-36473086 | Common:1; Rare:14 | ||||
| chr20:36541362-36541551 | Common:2; Rare:55 | ||||
| chr20:36573327-36573707 | Common:2; Rare:151 | ||||
| chr20:36605579-36605805 | Common:2; Rare:86 |