| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:45341037-45341615 | Common:4; Rare:259 | ||||
| chr13:46052696-46052812 | Common:1; Rare:33 | ||||
| chr13:46211796-46211935 | Common:1; Rare:49 | ||||
| chr13:46387232-46387352 | Rare:29 | ||||
| chr13:46553056-46553304 | Common:2; Rare:74 | ||||
| chr13:48037699-48037783 | Common:1; Rare:44 | ||||
| chr13:48233060-48233475 | Common:3; Rare:144 | ||||
| chr13:48303683-48303906 | Rare:70; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr13:48975676-48975934 | Common:2; Rare:81 | ||||
| chr13:48976339-48976824 | Common:3; Rare:147 | ||||
| chr13:49247807-49247994 | Rare:55 | ||||
| chr13:49444002-49444501 | Common:1; Rare:155 | ||||
| chr13:49496071-49496171 | Common:3; Rare:26 | ||||
| chr13:49936245-49936537 | Common:1; Rare:90 | ||||
| chr13:49996735-49997089 | Common:1; Rare:75 |