| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123416422-123416743 | Rare:87 | ||||
| chr8:123541071-123541378 | Common:3; Rare:99 | ||||
| chr8:124372672-124372839 | Common:1; Rare:59 | ||||
| chr8:124474526-124474772 | Rare:91 | ||||
| chr8:124474941-124475094 | Rare:48 | ||||
| chr8:124539052-124539189 | Common:2; Rare:73; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:125091622-125091944 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:126558346-126558628 | Common:1; Rare:104 | ||||
| chr8:127735873-127736076 | Rare:42 | ||||
| chr8:127736178-127736296 | Common:2; Rare:30 | ||||
| chr8:132675534-132675647 | Rare:32 | ||||
| chr8:133256588-133256889 | Common:2; Rare:82; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:133297132-133297521 | Common:3; Rare:150; Clinvar:4; Clinvar (benign):1 | ||||
| chr8:133571856-133572185 | Rare:81 | ||||
| chr8:134712997-134713205 | Common:1; Rare:68 |