| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44339208-44339480 | Common:3; Rare:80 | ||||
| chr21:44801737-44801883 | Rare:64 | ||||
| chr21:44873613-44874040 | Common:8; Rare:173 | ||||
| chr21:44939935-44940051 | Common:1; Rare:37 | ||||
| chr21:45287879-45288102 | Common:5; Rare:85 | ||||
| chr21:46184404-46184736 | Common:4; Rare:31 | ||||
| chr21:46286252-46286396 | Common:4; Rare:53 | ||||
| chr21:46286542-46286640 | Common:1; Rare:26 | ||||
| chr21:46323806-46324177 | Common:2; Rare:129; Clinvar:1; Clinvar (benign):1 | ||||
| chr21:46458684-46459023 | Common:3; Rare:117 | ||||
| chr21:46635487-46635737 | Common:5; Rare:82 | ||||
| chr22:17159141-17159385 | Common:7; Rare:114 | ||||
| chr22:17563297-17563476 | Common:2; Rare:36 | ||||
| chr22:17628698-17628897 | Common:1; Rare:72 | ||||
| chr22:17638696-17638817 | Rare:43 |