| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:103415053-103415476 | Common:6; Rare:223 | ||||
| chr8:108248659-108248836 | Rare:75 | ||||
| chr8:109334049-109334402 | Common:1; Rare:94 | ||||
| chr8:118110300-118110611 | Rare:72; Clinvar:1 | ||||
| chr8:119832826-119832897 | Common:1; Rare:25 | ||||
| chr8:120445072-120445431 | Common:1; Rare:92 | ||||
| chr8:123274248-123274331 | Rare:5 | ||||
| chr8:124474546-124474757 | Rare:75 | ||||
| chr8:124538981-124539276 | Common:2; Rare:154; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998200-124998514 | Common:1; Rare:121 | ||||
| chr8:133571953-133572253 | Rare:84 | ||||
| chr8:140511200-140511494 | Common:3; Rare:112 | ||||
| chr8:142669962-142670311 | Common:9; Rare:118 | ||||
| chr8:142727026-142727265 | Common:3; Rare:94 | ||||
| chr8:143018379-143018538 | Common:1; Rare:48 |