| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:102412698-102412980 | Common:3; Rare:70 | ||||
| chr8:102864146-102864486 | Common:2; Rare:135 | ||||
| chr8:103021016-103021132 | Rare:35 | ||||
| chr8:103298662-103298927 | Common:2; Rare:67 | ||||
| chr8:103415013-103415512 | Common:6; Rare:249 | ||||
| chr8:106657540-106657906 | Common:4; Rare:104 | ||||
| chr8:108248659-108248895 | Rare:98 | ||||
| chr8:108443463-108443653 | Common:3; Rare:80 | ||||
| chr8:109334006-109334402 | Common:1; Rare:116 | ||||
| chr8:109539665-109539908 | Rare:63 | ||||
| chr8:109540107-109540188 | Common:1; Rare:14 | ||||
| chr8:116755771-116755866 | Rare:60 | ||||
| chr8:116874390-116874449 | Rare:20 | ||||
| chr8:116874611-116874957 | Common:6; Rare:149; Clinvar (benign):1 | ||||
| chr8:117520584-117520778 | Common:4; Rare:44 |