| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:43789378-43789617 | Common:1; Rare:87 | ||||
| chr21:44339244-44339470 | Common:2; Rare:68 | ||||
| chr21:44873570-44874040 | Common:8; Rare:187 | ||||
| chr21:44939900-44940012 | Common:2; Rare:27 | ||||
| chr21:45287879-45288093 | Common:5; Rare:82 | ||||
| chr21:46184423-46184669 | Common:3; Rare:24 | ||||
| chr21:46286268-46286411 | Common:3; Rare:51 | ||||
| chr21:46323871-46324170 | Common:2; Rare:101; Clinvar:1; Clinvar (benign):1 | ||||
| chr22:17159175-17159373 | Common:6; Rare:90 | ||||
| chr22:17628687-17628877 | Common:1; Rare:67 | ||||
| chr22:17638696-17638819 | Rare:43 | ||||
| chr22:18077814-18078028 | Common:4; Rare:70; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19122389-19122650 | Common:3; Rare:60 | ||||
| chr22:19291686-19291969 | Common:10; Rare:93 | ||||
| chr22:19432294-19432616 | Common:4; Rare:136 |