| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:39387650-39387817 | Common:2; Rare:73 | ||||
| chr21:39445751-39445913 | Common:3; Rare:53 | ||||
| chr21:39451706-39452010 | Common:2; Rare:78 | ||||
| chr21:41316668-41316895 | Rare:49 | ||||
| chr21:41420062-41420335 | Common:4; Rare:65 | ||||
| chr21:41426061-41426326 | Common:3; Rare:56 | ||||
| chr21:41506771-41506909 | Rare:20 | ||||
| chr21:41507966-41508375 | Common:5; Rare:92 | ||||
| chr21:41766966-41767192 | Common:5; Rare:98; Clinvar:1; Clinvar (benign):2 | ||||
| chr21:41879295-41879575 | Common:5; Rare:87 | ||||
| chr21:42350500-42351040 | Common:8; Rare:133 | ||||
| chr21:42351042-42351084 | Rare:11 | ||||
| chr21:42351087-42351427 | Common:2; Rare:80 | ||||
| chr21:42366404-42366608 | Common:3; Rare:67 | ||||
| chr21:42496195-42496572 | Common:2; Rare:94 |