| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr13:98576219-98576308 | Common:1; Rare:29 | ||||
| chr13:98977794-98977897 | Common:1; Rare:30 | ||||
| chr13:98978341-98978628 | Common:3; Rare:43 | ||||
| chr13:99200667-99200900 | Common:6; Rare:109 | ||||
| chr13:100088901-100089122 | Rare:79; Clinvar:1; Clinvar (benign):2 | ||||
| chr13:100674765-100675060 | Common:3; Rare:120 | ||||
| chr13:102596773-102597045 | Common:1; Rare:126; Clinvar (benign):1 | ||||
| chr13:102773713-102773842 | Rare:60 | ||||
| chr13:102798939-102799130 | Common:1; Rare:40 | ||||
| chr13:106567835-106568261 | Rare:117 | ||||
| chr13:108218294-108218520 | Common:1; Rare:84 | ||||
| chr13:110305560-110305796 | Rare:41 | ||||
| chr13:110306948-110307526 | Common:7; Rare:179; Clinvar:3; Clinvar (benign):10 | ||||
| chr13:110307635-110307960 | Common:3; Rare:102 | ||||
| chr13:110430397-110430618 | Common:2; Rare:60; Clinvar (benign):3 |