| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124474190-124474326 | Common:1; Rare:31 | ||||
| chr8:124474987-124475231 | Rare:91 | ||||
| chr8:124539040-124539312 | Common:2; Rare:126; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124728391-124728621 | Rare:71 | ||||
| chr8:124998170-124998737 | Common:5; Rare:211 | ||||
| chr8:124998740-124998843 | Common:3; Rare:34 | ||||
| chr8:124998942-124999246 | Common:3; Rare:79 | ||||
| chr8:125091626-125091938 | Common:2; Rare:104; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:126558382-126558628 | Common:1; Rare:88 | ||||
| chr8:127735842-127736081 | Rare:56 | ||||
| chr8:127736130-127736269 | Common:3; Rare:29 | ||||
| chr8:132675518-132675677 | Rare:51 | ||||
| chr8:133297243-133297398 | Common:2; Rare:56; Clinvar:2 | ||||
| chr8:133570346-133570468 | Rare:30 | ||||
| chr8:133571817-133572185 | Rare:90 |