| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:98576985-98577593 | Common:4; Rare:187 | ||||
| chr13:98577619-98578000 | Common:2; Rare:89 | ||||
| chr13:98752555-98752764 | Common:2; Rare:57 | ||||
| chr13:98978030-98978152 | Common:1; Rare:24 | ||||
| chr13:99086214-99086230 | Rare:3 | ||||
| chr13:99086458-99086947 | Common:5; Rare:166 | ||||
| chr13:99200445-99200592 | Common:1; Rare:40 | ||||
| chr13:99200594-99200955 | Common:7; Rare:154 | ||||
| chr13:99201251-99201663 | Rare:146 | ||||
| chr13:99501182-99501535 | Common:1; Rare:106 | ||||
| chr13:99501633-99501851 | Rare:81 | ||||
| chr13:99606392-99606902 | Common:6; Rare:172 | ||||
| chr13:99981519-99981766 | Common:1; Rare:79 | ||||
| chr13:100088777-100089172 | Rare:151; Clinvar:2; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr13:100588458-100588498 | Rare:6 |