| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:123396388-123396557 | Common:2; Rare:74 | ||||
| chr8:124474969-124475121 | Rare:54 | ||||
| chr8:124539042-124539197 | Common:2; Rare:86; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124728400-124728706 | Common:4; Rare:91 | ||||
| chr8:125091683-125091914 | Common:2; Rare:78; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:126558362-126558628 | Common:1; Rare:100 | ||||
| chr8:127735884-127736287 | Common:3; Rare:87 | ||||
| chr8:130016388-130016468 | Rare:19 | ||||
| chr8:132675529-132675628 | Rare:30 | ||||
| chr8:133297248-133297481 | Common:2; Rare:94; Clinvar:2 | ||||
| chr8:133571788-133572163 | Common:1; Rare:91 | ||||
| chr8:140511270-140511494 | Common:1; Rare:93 | ||||
| chr8:141001136-141001344 | Common:2; Rare:69 | ||||
| chr8:142777814-142777917 | Rare:24 | ||||
| chr8:143018432-143018579 | Common:1; Rare:39 |