| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:22245026-22245452 | Common:2; Rare:151 | ||||
| chr8:23164022-23164258 | Rare:46 | ||||
| chr8:23225070-23225209 | Common:1; Rare:34 | ||||
| chr8:23457617-23457778 | Common:2; Rare:62 | ||||
| chr8:23528742-23529053 | Rare:96 | ||||
| chr8:24956070-24956183 | Rare:35; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:24956608-24956747 | Common:2; Rare:31 | ||||
| chr8:26291679-26291803 | Common:1; Rare:34 | ||||
| chr8:26382976-26383123 | Common:2; Rare:70 | ||||
| chr8:26383311-26383419 | Rare:27 | ||||
| chr8:26513855-26514221 | Common:1; Rare:83 | ||||
| chr8:27311242-27311591 | Common:8; Rare:121 | ||||
| chr8:27837736-27837910 | Rare:49 | ||||
| chr8:28490230-28490448 | Common:1; Rare:46 | ||||
| chr8:29263064-29263284 | Rare:68 |