| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:44989362-44989641 | Rare:118 | ||||
| chr13:45120180-45120590 | Common:2; Rare:100 | ||||
| chr13:45340907-45341536 | Common:6; Rare:278 | ||||
| chr13:45418322-45418516 | Rare:55 | ||||
| chr13:45464706-45465091 | Common:1; Rare:96 | ||||
| chr13:45615538-45615646 | Rare:23 | ||||
| chr13:45615712-45615805 | Rare:31 | ||||
| chr13:45851642-45851927 | Common:2; Rare:68 | ||||
| chr13:46052411-46052877 | Common:2; Rare:129 | ||||
| chr13:46553056-46553409 | Common:4; Rare:102 | ||||
| chr13:46797127-46797362 | Common:2; Rare:79 | ||||
| chr13:48001229-48001417 | Common:1; Rare:86; Clinvar:3; Clinvar (benign):6 | ||||
| chr13:48037699-48037820 | Common:2; Rare:62; Clinvar:2 | ||||
| chr13:48037912-48038091 | Common:5; Rare:61 | ||||
| chr13:48233053-48233227 | Common:1; Rare:58 |