| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124539042-124539222 | Common:2; Rare:97; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124998176-124998531 | Common:1; Rare:135 | ||||
| chr8:125091614-125091910 | Common:2; Rare:94; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:127736119-127736269 | Common:3; Rare:30 | ||||
| chr8:129939719-129940043 | Common:1; Rare:109 | ||||
| chr8:130016390-130016753 | Common:3; Rare:105 | ||||
| chr8:133499390-133499534 | Common:2; Rare:25 | ||||
| chr8:134713025-134713155 | Common:1; Rare:45 | ||||
| chr8:140511231-140511490 | Common:3; Rare:103 | ||||
| chr8:141001214-141001431 | Common:1; Rare:79 | ||||
| chr8:143246745-143246965 | Rare:71 | ||||
| chr8:143541430-143541663 | Common:3; Rare:75 | ||||
| chr8:143558262-143558390 | Common:1; Rare:48 | ||||
| chr8:143597098-143597240 | Common:1; Rare:46 | ||||
| chr8:143609555-143609847 | Common:4; Rare:90 |