| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:132910509-132910635 | Common:2; Rare:16 | ||||
| chr8:132912515-132912617 | Rare:16 | ||||
| chr8:132912917-132913451 | Common:3; Rare:142; Clinvar:4 | ||||
| chr8:132913511-132913960 | Common:2; Rare:81 | ||||
| chr8:132913964-132914266 | Common:1; Rare:48 | ||||
| chr8:132914385-132915002 | Common:6; Rare:97 | ||||
| chr8:132915330-132915669 | Rare:66 | ||||
| chr8:132918098-132918284 | Rare:46 | ||||
| chr8:132918296-132918911 | Common:5; Rare:101 | ||||
| chr8:132920940-132921144 | Common:4; Rare:37 | ||||
| chr8:132921970-132922151 | Common:1; Rare:22 | ||||
| chr8:132923126-132923602 | Common:2; Rare:127; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr8:132926012-132926282 | Rare:45 | ||||
| chr8:132933278-132933749 | Common:9; Rare:98; Clinvar:1 | ||||
| chr8:132935110-132935209 | Rare:18 |