| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:106657548-106657949 | Common:5; Rare:117 | ||||
| chr8:106658172-106658461 | Common:2; Rare:68 | ||||
| chr8:108248613-108248839 | Rare:86 | ||||
| chr8:108443463-108443672 | Common:3; Rare:93 | ||||
| chr8:108443929-108443983 | Rare:11 | ||||
| chr8:109334009-109334412 | Common:1; Rare:117 | ||||
| chr8:109362348-109362625 | Common:1; Rare:64 | ||||
| chr8:109539488-109539915 | Common:2; Rare:108 | ||||
| chr8:109540062-109540216 | Common:1; Rare:33 | ||||
| chr8:109540510-109540642 | Common:1; Rare:29 | ||||
| chr8:109644665-109644998 | Common:2; Rare:100 | ||||
| chr8:116755777-116755894 | Common:1; Rare:62 | ||||
| chr8:116874165-116874282 | Rare:38 | ||||
| chr8:116874611-116874959 | Common:6; Rare:150; Clinvar (benign):1 | ||||
| chr8:117520584-117520874 | Common:6; Rare:72 |