| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:20567046-20567219 | Common:1; Rare:58 | ||||
| chr13:20773931-20774042 | Rare:37 | ||||
| chr13:21140134-21140618 | Rare:175 | ||||
| chr13:21176482-21176717 | Common:2; Rare:107 | ||||
| chr13:21603816-21603923 | Rare:45 | ||||
| chr13:21604042-21604295 | Common:5; Rare:130 | ||||
| chr13:21670861-21671162 | Common:1; Rare:93; Clinvar:1; Clinvar (benign):1 | ||||
| chr13:21674053-21674277 | Rare:41 | ||||
| chr13:23433429-23433511 | Rare:10 | ||||
| chr13:23579240-23579396 | Common:3; Rare:49 | ||||
| chr13:23889268-23889484 | Common:1; Rare:76 | ||||
| chr13:23980260-23980412 | Common:1; Rare:40 | ||||
| chr13:24160571-24160860 | Common:2; Rare:81 | ||||
| chr13:24512747-24512849 | Common:3; Rare:32 | ||||
| chr13:24922788-24923049 | Common:1; Rare:82; Clinvar:1 |