| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:36156151-36157138 | Common:66; Rare:1732 | ||||
| chr21:36164339-36164739 | Common:3; Rare:168 | ||||
| chr21:36319894-36320445 | Common:28; Rare:1083 | ||||
| chr21:36320496-36321206 | Common:4; Rare:236 | ||||
| chr21:36385010-36385500 | Common:1; Rare:382 | ||||
| chr21:36385895-36386295 | Rare:196 | ||||
| chr21:36966250-36966553 | Common:11; Rare:381 | ||||
| chr21:36966503-36967070 | Common:28; Rare:502 | ||||
| chr21:36989710-36990080 | Common:22; Rare:322 | ||||
| chr21:36990021-36990690 | Common:38; Rare:447; Clinvar:2; Clinvar (benign):29 | ||||
| chr21:37071389-37072135 | Common:2; Rare:162 | ||||
| chr21:37072346-37072821 | Common:25; Rare:508; Clinvar (pathogenic):1 | ||||
| chr21:37072870-37073440 | Common:40; Rare:1082 | ||||
| chr21:37073472-37074013 | Common:12; Rare:189 | ||||
| chr21:37266634-37266980 | Rare:114 |