| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr22:37149914-37150151 | Rare:47 | ||||
| chr22:37231903-37231965 | Rare:20 | ||||
| chr22:37244141-37244342 | Rare:57 | ||||
| chr22:37608679-37609053 | Common:2; Rare:108 | ||||
| chr22:37675564-37675642 | Rare:18 | ||||
| chr22:37676556-37676861 | Common:1; Rare:63 | ||||
| chr22:37677282-37677441 | Common:2; Rare:41 | ||||
| chr22:37849320-37849462 | Rare:80 | ||||
| chr22:38656387-38656715 | Common:1; Rare:74 | ||||
| chr22:38681817-38681957 | Common:1; Rare:53 | ||||
| chr22:39040655-39040893 | Common:1; Rare:48 | ||||
| chr22:39319607-39319791 | Common:2; Rare:81 | ||||
| chr22:40346441-40346551 | Rare:45; Clinvar:2; Clinvar (benign):1 | ||||
| chr22:40370521-40370683 | Rare:67 | ||||
| chr22:40856924-40857154 | Common:1; Rare:92; Clinvar:3 |