| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:19171606-19171724 | Rare:37 | ||||
| chr22:19176430-19176586 | Rare:75; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr22:19455745-19455886 | Common:1; Rare:37 | ||||
| chr22:19758652-19758780 | Rare:38 | ||||
| chr22:20125185-20125367 | Common:1; Rare:48 | ||||
| chr22:20702618-20702838 | Common:2; Rare:50 | ||||
| chr22:20956907-20957121 | Common:1; Rare:40 | ||||
| chr22:21014236-21014416 | Rare:47 | ||||
| chr22:22098555-22098742 | Common:1; Rare:45 | ||||
| chr22:22297924-22298210 | Common:13; Rare:115 | ||||
| chr22:22306813-22306974 | Common:3; Rare:39 | ||||
| chr22:22369486-22369639 | Common:2; Rare:47 | ||||
| chr22:22380631-22380890 | Common:2; Rare:86 | ||||
| chr22:22394892-22395043 | Rare:44 | ||||
| chr22:22900972-22901238 | Common:2; Rare:105 |