| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:18084770-18084859 | Common:1; Rare:46; Clinvar (benign):1 | ||||
| chr8:18084925-18084941 | Rare:5 | ||||
| chr8:18084943-18085015 | Rare:14 | ||||
| chr8:19938784-19938956 | Rare:40 | ||||
| chr8:20197215-20197481 | Common:2; Rare:131 | ||||
| chr8:21912504-21912617 | Common:1; Rare:33 | ||||
| chr8:21919627-21919773 | Common:2; Rare:65 | ||||
| chr8:22245024-22245192 | Common:1; Rare:83 | ||||
| chr8:22999769-22999936 | Rare:35 | ||||
| chr8:23224895-23225227 | Common:2; Rare:96 | ||||
| chr8:23457613-23457789 | Common:3; Rare:62 | ||||
| chr8:26045350-26045537 | Common:2; Rare:72 | ||||
| chr8:26382928-26383233 | Common:3; Rare:137 | ||||
| chr8:26383304-26383477 | Rare:46 | ||||
| chr8:26383491-26383671 | Common:2; Rare:39 |