| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:108443472-108443665 | Common:2; Rare:87 | ||||
| chr8:109334104-109334400 | Common:1; Rare:64 | ||||
| chr8:117520521-117520769 | Common:5; Rare:57 | ||||
| chr8:118951883-118952157 | Common:1; Rare:72; Clinvar:7; Clinvar (benign):1 | ||||
| chr8:119832830-119832916 | Common:1; Rare:28 | ||||
| chr8:120445097-120445454 | Common:1; Rare:89 | ||||
| chr8:124474959-124475094 | Rare:45 | ||||
| chr8:124539050-124539224 | Common:2; Rare:90; Clinvar (benign):7; Clinvar (pathogenic):1 | ||||
| chr8:125091755-125091914 | Common:1; Rare:51 | ||||
| chr8:126558353-126558628 | Common:1; Rare:103 | ||||
| chr8:129939752-129939872 | Common:1; Rare:43 | ||||
| chr8:140511195-140511499 | Common:3; Rare:114 | ||||
| chr8:140718575-140718895 | Rare:53 | ||||
| chr8:141001202-141001478 | Common:2; Rare:103 | ||||
| chr8:141391881-141392073 | Common:1; Rare:69 |