| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:6708155-6708373 | Common:3; Rare:89 | ||||
| chr8:9555712-9556056 | Common:5; Rare:156 | ||||
| chr8:9679592-9679870 | Rare:81 | ||||
| chr8:10054651-10054851 | Common:1; Rare:107 | ||||
| chr8:10839824-10839937 | Rare:48 | ||||
| chr8:11201789-11201917 | Rare:36 | ||||
| chr8:11284229-11284521 | Common:2; Rare:103 | ||||
| chr8:11284639-11284869 | Common:2; Rare:91 | ||||
| chr8:11285063-11285143 | Common:1; Rare:36 | ||||
| chr8:11466711-11466914 | Common:1; Rare:78 | ||||
| chr8:11769570-11769781 | Common:5; Rare:91 | ||||
| chr8:11802411-11802806 | Common:7; Rare:224 | ||||
| chr8:12753936-12754184 | Common:1; Rare:86 | ||||
| chr8:15540137-15540449 | Common:5; Rare:118; Clinvar:11; Clinvar (benign):1 | ||||
| chr8:17027649-17027744 | Rare:32 |