| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:132999325-132999503 | Common:3; Rare:32 | ||||
| chr8:132999855-133000596 | Common:3; Rare:122 | ||||
| chr8:133005398-133005979 | Common:1; Rare:101 | ||||
| chr8:133010640-133010919 | Common:3; Rare:52 | ||||
| chr8:133011721-133012040 | Common:2; Rare:86; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:133012457-133013353 | Common:5; Rare:147 | ||||
| chr8:133013531-133013832 | Common:2; Rare:93 | ||||
| chr8:133024216-133024315 | Rare:22 | ||||
| chr8:133026798-133026910 | Rare:29 | ||||
| chr8:133028625-133029030 | Common:1; Rare:77 | ||||
| chr8:133029799-133030339 | Common:2; Rare:158; Clinvar:3; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:133032196-133032231 | Rare:7 | ||||
| chr8:133033190-133033385 | Common:1; Rare:29 | ||||
| chr8:133034481-133034734 | Common:3; Rare:40 | ||||
| chr8:133035086-133035367 | Common:1; Rare:42 |