| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:116874611-116874930 | Common:6; Rare:134; Clinvar (benign):1 | ||||
| chr8:117520526-117520753 | Common:5; Rare:50 | ||||
| chr8:118951883-118952157 | Common:1; Rare:72; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832829-119832877 | Common:1; Rare:15 | ||||
| chr8:120445100-120445421 | Common:1; Rare:76 | ||||
| chr8:124474987-124475099 | Rare:37 | ||||
| chr8:124539052-124539198 | Common:2; Rare:78; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr8:124998210-124998560 | Common:1; Rare:137 | ||||
| chr8:125091707-125091914 | Common:2; Rare:73; Clinvar:1; Clinvar (benign):3 | ||||
| chr8:127736015-127736261 | Common:3; Rare:48 | ||||
| chr8:140511257-140511495 | Common:2; Rare:98 | ||||
| chr8:141001144-141001429 | Common:2; Rare:94 | ||||
| chr8:143018432-143018546 | Rare:30 | ||||
| chr8:143541459-143541658 | Common:2; Rare:57 | ||||
| chr8:143635902-143636061 | Common:2; Rare:67 |