| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:99992017-99992246 | Common:1; Rare:44 | ||||
| chr13:99992554-99992580 | Rare:4 | ||||
| chr13:99992845-99993149 | Common:1; Rare:63 | ||||
| chr13:99993920-99994122 | Common:2; Rare:36 | ||||
| chr13:99995201-99995210 | Rare:1 | ||||
| chr13:99995648-99995740 | Common:1; Rare:19 | ||||
| chr13:99995872-99995940 | Rare:18 | ||||
| chr13:99996276-99996304 | Rare:2 | ||||
| chr13:100132242-100132347 | Common:2; Rare:33 | ||||
| chr13:100234129-100234226 | Rare:18 | ||||
| chr13:100234269-100234326 | Rare:13 | ||||
| chr13:100235732-100235925 | Common:2; Rare:50; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:100294164-100294297 | Rare:26 | ||||
| chr13:100298236-100298284 | Rare:6 | ||||
| chr13:100298319-100298405 | Common:1; Rare:21 |