| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:41420196-41420335 | Common:2; Rare:39 | ||||
| chr21:41426096-41426262 | Common:3; Rare:37 | ||||
| chr21:42496200-42496583 | Common:2; Rare:95 | ||||
| chr21:42653443-42653765 | Common:5; Rare:45 | ||||
| chr21:42879522-42879625 | Common:3; Rare:40 | ||||
| chr21:42893064-42893378 | Common:4; Rare:112 | ||||
| chr21:43659468-43659636 | Common:1; Rare:55 | ||||
| chr21:43776256-43776379 | Common:1; Rare:49; Clinvar:2; Clinvar (benign):8; Clinvar (pathogenic):2 | ||||
| chr21:44299958-44300108 | Common:1; Rare:59; Clinvar (benign):1 | ||||
| chr21:44339190-44339438 | Common:2; Rare:83 | ||||
| chr21:44350174-44350260 | Common:1; Rare:26 | ||||
| chr21:44801739-44801847 | Rare:56 | ||||
| chr21:44873672-44874053 | Common:7; Rare:153 | ||||
| chr21:45287879-45288102 | Common:5; Rare:85 | ||||
| chr21:45981524-45981914 | Common:24; Rare:99; Clinvar:3; Clinvar (benign):3 |