| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:27479098-27479364 | Common:10; Rare:61; Clinvar:10; Clinvar (benign):6 | ||||
| chr8:27490971-27491219 | Common:3; Rare:82 | ||||
| chr8:27610474-27610757 | Common:1; Rare:95 | ||||
| chr8:27611331-27611599 | Common:3; Rare:53 | ||||
| chr8:27611608-27611662 | Common:1; Rare:13 | ||||
| chr8:27611667-27611736 | Rare:16 | ||||
| chr8:27611738-27612009 | Common:1; Rare:51 | ||||
| chr8:27772567-27772722 | Common:5; Rare:53 | ||||
| chr8:27774254-27774565 | Common:3; Rare:63; Clinvar (benign):1 | ||||
| chr8:27837758-27837886 | Rare:35 | ||||
| chr8:28092787-28093248 | Common:4; Rare:139 | ||||
| chr8:28490179-28490424 | Rare:45 | ||||
| chr8:28494100-28494328 | Common:5; Rare:79 | ||||
| chr8:28701251-28701647 | Common:3; Rare:133 | ||||
| chr8:28889905-28890678 | Rare:211 |