| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:44873506-44873572 | Rare:18 | ||||
| chr21:44873605-44874018 | Common:8; Rare:171 | ||||
| chr21:45287879-45288085 | Common:5; Rare:80 | ||||
| chr21:45981519-45981838 | Common:23; Rare:77; Clinvar (benign):2 | ||||
| chr21:45986667-45986989 | Common:5; Rare:109; Clinvar:11; Clinvar (benign):9 | ||||
| chr21:46184423-46184749 | Common:4; Rare:29 | ||||
| chr21:46286233-46286370 | Common:3; Rare:53 | ||||
| chr21:46323884-46324153 | Common:2; Rare:92; Clinvar (benign):1 | ||||
| chr21:46458708-46459063 | Common:3; Rare:121 | ||||
| chr21:46635457-46635731 | Common:6; Rare:94 | ||||
| chr22:17159175-17159375 | Common:6; Rare:91 | ||||
| chr22:17628606-17628872 | Common:2; Rare:87 | ||||
| chr22:17638696-17638830 | Rare:49 | ||||
| chr22:18150075-18150179 | Common:1; Rare:32 | ||||
| chr22:19122385-19122667 | Common:4; Rare:67 |