| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:21333784-21334184 | Common:1; Rare:95 | ||||
| chr20:21357584-21357764 | Rare:44 | ||||
| chr20:21488243-21488316 | Rare:13 | ||||
| chr20:22763673-22763862 | Common:2; Rare:32 | ||||
| chr20:22827993-22828084 | Rare:21 | ||||
| chr20:23047229-23047271 | Rare:6; Clinvar (benign):1 | ||||
| chr20:23047361-23047515 | Common:3; Rare:34; Clinvar (benign):5 | ||||
| chr20:23095053-23095249 | Common:1; Rare:31 | ||||
| chr20:23097070-23097282 | Common:2; Rare:47 | ||||
| chr20:23100473-23100740 | Common:1; Rare:47 | ||||
| chr20:23395086-23395215 | Rare:35 | ||||
| chr20:25278873-25279148 | Common:2; Rare:83 | ||||
| chr20:25687604-25687909 | Common:1; Rare:52 | ||||
| chr20:26009478-26009807 | Common:1; Rare:79 | ||||
| chr20:26116771-26116791 | Rare:2 |