| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:103298737-103298900 | Common:1; Rare:38 | ||||
| chr8:103371406-103371636 | Common:1; Rare:72 | ||||
| chr8:103415064-103415444 | Common:6; Rare:199 | ||||
| chr8:108248675-108248867 | Rare:79 | ||||
| chr8:109334078-109334449 | Common:1; Rare:99 | ||||
| chr8:116755789-116755937 | Common:1; Rare:70 | ||||
| chr8:119832826-119832891 | Common:1; Rare:24 | ||||
| chr8:120445098-120445397 | Common:1; Rare:69 | ||||
| chr8:123274236-123274324 | Rare:8 | ||||
| chr8:124474562-124474788 | Rare:83 | ||||
| chr8:124538988-124539278 | Common:2; Rare:152; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091712-125091894 | Common:2; Rare:63; Clinvar (benign):3 | ||||
| chr8:133571924-133572289 | Rare:97 | ||||
| chr8:140511026-140511353 | Common:3; Rare:106 | ||||
| chr8:141128298-141128648 | Common:4; Rare:106 |