| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:93700502-93700642 | Common:1; Rare:59 | ||||
| chr8:93740980-93741188 | Common:1; Rare:67 | ||||
| chr8:94553449-94553761 | Common:3; Rare:109 | ||||
| chr8:94719730-94719945 | Common:1; Rare:59 | ||||
| chr8:96261544-96261957 | Common:6; Rare:142 | ||||
| chr8:98045506-98045626 | Common:2; Rare:46 | ||||
| chr8:98117144-98117317 | Common:2; Rare:58 | ||||
| chr8:99013000-99013315 | Rare:61 | ||||
| chr8:100150565-100150670 | Rare:32 | ||||
| chr8:100309987-100310306 | Common:1; Rare:121 | ||||
| chr8:101205546-101205878 | Common:4; Rare:106 | ||||
| chr8:103298682-103298916 | Common:1; Rare:62 | ||||
| chr8:103415065-103415464 | Common:6; Rare:209 | ||||
| chr8:109334060-109334400 | Common:1; Rare:85 | ||||
| chr8:118951875-118952149 | Common:1; Rare:71; Clinvar:7; Clinvar (benign):1 |