| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:31093163-31093388 | Common:1; Rare:45 | ||||
| chr22:31098663-31099179 | Common:2; Rare:162 | ||||
| chr22:31105275-31105563 | Rare:56 | ||||
| chr22:31107417-31107913 | Common:2; Rare:145 | ||||
| chr22:31122740-31122994 | Common:3; Rare:65 | ||||
| chr22:31290718-31290937 | Rare:92 | ||||
| chr22:31292389-31292632 | Common:1; Rare:52 | ||||
| chr22:31399445-31399685 | Rare:72 | ||||
| chr22:31489768-31490106 | Common:1; Rare:134 | ||||
| chr22:31496409-31496556 | Common:1; Rare:37 | ||||
| chr22:31630809-31631068 | Common:7; Rare:63 | ||||
| chr22:31753725-31754054 | Common:1; Rare:114 | ||||
| chr22:31944837-31945027 | Common:3; Rare:66 | ||||
| chr22:32801836-32802135 | Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:35257369-35257529 | Common:1; Rare:43 |