| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:106657539-106657930 | Common:5; Rare:113 | ||||
| chr8:108248614-108248862 | Rare:94 | ||||
| chr8:108443463-108443661 | Common:3; Rare:85 | ||||
| chr8:108787545-108787717 | Common:1; Rare:42 | ||||
| chr8:109334056-109334406 | Common:1; Rare:90 | ||||
| chr8:109539635-109539916 | Rare:76 | ||||
| chr8:109540108-109540407 | Common:3; Rare:65 | ||||
| chr8:109540521-109540634 | Common:1; Rare:22 | ||||
| chr8:109643937-109644129 | Common:2; Rare:41 | ||||
| chr8:109644670-109644907 | Common:1; Rare:74 | ||||
| chr8:116755738-116755956 | Common:1; Rare:109 | ||||
| chr8:116874383-116874678 | Common:2; Rare:77; Clinvar (benign):1 | ||||
| chr8:116874748-116874957 | Common:5; Rare:105 | ||||
| chr8:117520584-117520909 | Common:6; Rare:90 | ||||
| chr8:118951823-118952133 | Common:1; Rare:89; Clinvar:7; Clinvar (benign):1 |