| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr21:46323830-46324153 | Common:2; Rare:108; Clinvar (benign):1 | ||||
| chr21:46635465-46635737 | Common:5; Rare:91 | ||||
| chr22:17628698-17628853 | Common:1; Rare:52 | ||||
| chr22:17638668-17638811 | Rare:49 | ||||
| chr22:19178462-19178519 | Common:1; Rare:13 | ||||
| chr22:19447677-19447833 | Common:1; Rare:66 | ||||
| chr22:19479107-19479477 | Common:4; Rare:137 | ||||
| chr22:19479661-19479956 | Common:5; Rare:76 | ||||
| chr22:19854787-19855013 | Rare:83 | ||||
| chr22:19881079-19881506 | Common:4; Rare:110 | ||||
| chr22:19941764-19941886 | Rare:49; Clinvar:2 | ||||
| chr22:20117252-20117557 | Common:3; Rare:92 | ||||
| chr22:20319998-20320104 | Common:1; Rare:42 | ||||
| chr22:21002088-21002195 | Common:3; Rare:37 | ||||
| chr22:21952807-21952990 | Common:1; Rare:65 |