| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:27633787-27634002 | Common:4; Rare:123 | ||||
| chr8:27772563-27772725 | Common:9; Rare:93 | ||||
| chr8:27774292-27774606 | Common:2; Rare:74; Clinvar:3; Clinvar (benign):1 | ||||
| chr8:27837701-27837941 | Common:4; Rare:136 | ||||
| chr8:28093026-28093246 | Common:2; Rare:125 | ||||
| chr8:28093260-28093570 | Common:2; Rare:71 | ||||
| chr8:28386272-28386642 | Common:16; Rare:129 | ||||
| chr8:28490209-28490450 | Common:2; Rare:97 | ||||
| chr8:28494092-28494321 | Common:9; Rare:127 | ||||
| chr8:28622251-28622886 | Common:7; Rare:346 | ||||
| chr8:28701399-28701639 | Common:3; Rare:161 | ||||
| chr8:28889891-28890690 | Rare:373 | ||||
| chr8:28891137-28891537 | Rare:118 | ||||
| chr8:29263026-29263284 | Rare:145 | ||||
| chr8:29350635-29351010 | Common:5; Rare:168 |