| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:124450732-124450832 | Common:3; Rare:33 | ||||
| chr8:124474521-124474767 | Common:1; Rare:92 | ||||
| chr8:124474946-124475099 | Rare:48 | ||||
| chr8:124538972-124539287 | Common:2; Rare:164; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:124539380-124539496 | Rare:28 | ||||
| chr8:124728421-124728750 | Common:4; Rare:102 | ||||
| chr8:124973119-124973388 | Rare:62 | ||||
| chr8:124998176-124998718 | Common:5; Rare:208 | ||||
| chr8:125091617-125091947 | Common:2; Rare:105; Clinvar:1; Clinvar (benign):4 | ||||
| chr8:125429712-125430033 | Common:1; Rare:93 | ||||
| chr8:129939609-129940104 | Common:1; Rare:168 | ||||
| chr8:130016624-130016775 | Common:1; Rare:47 | ||||
| chr8:130443586-130443910 | Common:4; Rare:95 | ||||
| chr8:132675529-132675652 | Rare:35 | ||||
| chr8:133571885-133572241 | Rare:93 |