| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:38787015-38787279 | Rare:99 | ||||
| chr8:38996453-38997155 | Common:8; Rare:262; Clinvar (benign):1 | ||||
| chr8:42541555-42541619 | Rare:17 | ||||
| chr8:42541621-42541770 | Rare:57 | ||||
| chr8:42896573-42897010 | Common:1; Rare:179 | ||||
| chr8:43056238-43056466 | Rare:87 | ||||
| chr8:43140284-43140468 | Common:2; Rare:78; Clinvar:4 | ||||
| chr8:47260787-47260983 | Common:3; Rare:85 | ||||
| chr8:48008362-48008457 | Common:1; Rare:63 | ||||
| chr8:51899061-51899284 | Common:3; Rare:102 | ||||
| chr8:52714408-52714567 | Common:1; Rare:65 | ||||
| chr8:55773309-55773474 | Common:2; Rare:49 | ||||
| chr8:56074412-56074697 | Common:4; Rare:117 | ||||
| chr8:58553075-58553283 | Rare:72 | ||||
| chr8:58659329-58659493 | Common:1; Rare:62 |