| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:26254026-26254247 | Rare:61 | ||||
| chr13:27171037-27171279 | Common:3; Rare:59 | ||||
| chr13:27171450-27171499 | Rare:17 | ||||
| chr13:27171742-27172143 | Common:1; Rare:148 | ||||
| chr13:27251199-27251830 | Common:12; Rare:199 | ||||
| chr13:27270642-27270865 | Common:1; Rare:80 | ||||
| chr13:27424455-27424742 | Common:5; Rare:96 | ||||
| chr13:27449962-27450346 | Common:3; Rare:121 | ||||
| chr13:27450487-27450695 | Common:2; Rare:79 | ||||
| chr13:27450992-27451026 | Rare:5 | ||||
| chr13:27620005-27620092 | Common:1; Rare:20 | ||||
| chr13:27620423-27620862 | Common:4; Rare:149 | ||||
| chr13:27621782-27621945 | Common:4; Rare:80; Clinvar:5; Clinvar (benign):5 | ||||
| chr13:28100531-28100745 | Common:3; Rare:51 | ||||
| chr13:28137937-28138313 | Common:4; Rare:98 |