| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124474517-124474782 | Common:1; Rare:97 | ||||
| chr8:124474944-124475242 | Rare:105 | ||||
| chr8:124504323-124504584 | Common:2; Rare:50 | ||||
| chr8:124538981-124539286 | Common:2; Rare:157; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124999009-124999180 | Common:1; Rare:42 | ||||
| chr8:125091617-125091938 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:127735231-127735536 | Rare:51 | ||||
| chr8:127735903-127736626 | Common:4; Rare:190 | ||||
| chr8:129939610-129939866 | Common:1; Rare:92 | ||||
| chr8:130443473-130443777 | Common:5; Rare:83 | ||||
| chr8:133297138-133297532 | Common:3; Rare:153; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133571810-133572351 | Common:1; Rare:138 | ||||
| chr8:140457696-140457890 | Common:4; Rare:57 | ||||
| chr8:140511026-140511543 | Common:4; Rare:175 | ||||
| chr8:140511718-140512000 | Common:3; Rare:106 |