| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:27311226-27311695 | Common:10; Rare:154 | ||||
| chr8:27491010-27491256 | Common:3; Rare:94 | ||||
| chr8:27611671-27611790 | Rare:28 | ||||
| chr8:27614687-27614949 | Rare:86 | ||||
| chr8:27772527-27772782 | Common:7; Rare:83 | ||||
| chr8:27774238-27774606 | Common:3; Rare:85; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:27837701-27837941 | Common:2; Rare:71 | ||||
| chr8:28092779-28093285 | Common:4; Rare:157 | ||||
| chr8:28490214-28490431 | Common:1; Rare:42 | ||||
| chr8:28494065-28494334 | Common:5; Rare:96 | ||||
| chr8:28701238-28701639 | Common:3; Rare:133 | ||||
| chr8:28889890-28890686 | Rare:220 | ||||
| chr8:29263064-29263244 | Rare:58 | ||||
| chr8:30082939-30083389 | Common:2; Rare:141 | ||||
| chr8:30095294-30095517 | Common:2; Rare:70 |