| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:17396258-17396534 | Common:4; Rare:74 | ||||
| chr22:17702089-17702396 | Rare:81 | ||||
| chr22:17731047-17731086 | Rare:6 | ||||
| chr22:17929289-17929516 | Rare:38 | ||||
| chr22:18986213-18986497 | Common:3; Rare:47 | ||||
| chr22:19108303-19108562 | Common:1; Rare:47 | ||||
| chr22:19171606-19171729 | Rare:39 | ||||
| chr22:19263282-19263541 | Common:2; Rare:46 | ||||
| chr22:19351355-19351513 | Rare:33 | ||||
| chr22:19382878-19383124 | Common:2; Rare:42 | ||||
| chr22:19404092-19404157 | Common:1; Rare:11 | ||||
| chr22:19405318-19405338 | Rare:1 | ||||
| chr22:19434568-19434764 | Rare:41 | ||||
| chr22:19446623-19446701 | Common:1; Rare:22 | ||||
| chr22:19483494-19484006 | Rare:117; Clinvar:1; Clinvar (pathogenic):1 |