| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36990187-36990254 | Common:3; Rare:22; Clinvar (benign):3 | ||||
| chr21:37072532-37072741 | Common:5; Rare:106 | ||||
| chr21:37072998-37073390 | Common:5; Rare:149 | ||||
| chr21:37267289-37267704 | Common:4; Rare:149 | ||||
| chr21:37267905-37267969 | Rare:27 | ||||
| chr21:39183291-39183594 | Common:7; Rare:116 | ||||
| chr21:39348637-39348959 | Common:1; Rare:122 | ||||
| chr21:39348966-39349410 | Common:18; Rare:133 | ||||
| chr21:39380185-39380442 | Common:1; Rare:116 | ||||
| chr21:39387650-39387827 | Common:2; Rare:76 | ||||
| chr21:39445742-39445925 | Common:3; Rare:60 | ||||
| chr21:41767046-41767173 | Common:3; Rare:60; Clinvar:1 | ||||
| chr21:41879295-41879555 | Common:5; Rare:84 | ||||
| chr21:42513617-42513906 | Rare:83 | ||||
| chr21:42514396-42514560 | Rare:35 |