| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44873622-44874040 | Common:8; Rare:168 | ||||
| chr21:45287879-45288085 | Common:5; Rare:80 | ||||
| chr21:46184423-46184709 | Common:3; Rare:24 | ||||
| chr21:46286222-46286399 | Common:4; Rare:66 | ||||
| chr21:46286573-46286684 | Common:1; Rare:38 | ||||
| chr21:46323840-46324222 | Common:3; Rare:139; Clinvar:3; Clinvar (benign):2 | ||||
| chr21:46635487-46635737 | Common:5; Rare:82 | ||||
| chr22:17159200-17159350 | Common:4; Rare:71 | ||||
| chr22:17628688-17628878 | Common:1; Rare:68 | ||||
| chr22:17638696-17638830 | Rare:49 | ||||
| chr22:18077713-18078030 | Common:5; Rare:90; Clinvar:3; Clinvar (benign):2 | ||||
| chr22:19432378-19432606 | Common:2; Rare:95 | ||||
| chr22:19447667-19447774 | Common:1; Rare:55 | ||||
| chr22:19479107-19479463 | Common:4; Rare:130 | ||||
| chr22:19479687-19479956 | Common:4; Rare:72 |