| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr20:23637140-23637510 | Common:4; Rare:132 | ||||
| chr20:23637789-23638133 | Common:19; Rare:254; Clinvar (benign):3 | ||||
| chr20:24469301-24470030 | Common:4; Rare:398 | ||||
| chr20:24992585-24992987 | Common:22; Rare:417 | ||||
| chr20:25058048-25058438 | Common:10; Rare:153 | ||||
| chr20:25195552-25196340 | Common:21; Rare:408 | ||||
| chr20:25247893-25248399 | Common:5; Rare:487 | ||||
| chr20:25310204-25311110 | Common:3; Rare:300 | ||||
| chr20:25390250-25390690 | Common:33; Rare:377; Clinvar:1 | ||||
| chr20:25390632-25391159 | Common:15; Rare:506; Clinvar:13; Clinvar (benign):9 | ||||
| chr20:25407476-25407830 | Common:8; Rare:318; Clinvar (pathogenic):3 | ||||
| chr20:25585080-25585352 | Common:4; Rare:175 | ||||
| chr20:25585399-25585752 | Common:9; Rare:227 | ||||
| chr20:25623646-25624310 | Common:4; Rare:553 | ||||
| chr20:25624352-25624586 | Common:3; Rare:115 |