| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31160114-31160232 | Common:1; Rare:45 | ||||
| chr22:31212109-31212312 | Rare:66 | ||||
| chr22:31290718-31290911 | Rare:79 | ||||
| chr22:31292429-31292758 | Common:1; Rare:62 | ||||
| chr22:31346560-31346856 | Common:6; Rare:68 | ||||
| chr22:31399452-31399660 | Rare:58 | ||||
| chr22:31496373-31496565 | Common:2; Rare:50 | ||||
| chr22:31630829-31630978 | Common:4; Rare:38 | ||||
| chr22:31662212-31662377 | Common:2; Rare:63 | ||||
| chr22:31749821-31749869 | Common:1; Rare:7 | ||||
| chr22:31750021-31750332 | Common:3; Rare:88 | ||||
| chr22:31753765-31754087 | Common:1; Rare:115 | ||||
| chr22:31792573-31792687 | Common:2; Rare:20 | ||||
| chr22:32474636-32474990 | Common:4; Rare:110; Clinvar:6; Clinvar (benign):2 | ||||
| chr22:35257367-35257509 | Common:1; Rare:31 |