| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17922608-17923006 | Common:5; Rare:156 | ||||
| chr8:18084763-18085007 | Common:3; Rare:91; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr8:19013597-19013992 | Common:6; Rare:120 | ||||
| chr8:19817204-19817522 | Common:6; Rare:113 | ||||
| chr8:22089088-22089231 | Rare:51 | ||||
| chr8:22141806-22142015 | Common:2; Rare:66 | ||||
| chr8:22245018-22245459 | Common:2; Rare:159 | ||||
| chr8:22367053-22367324 | Common:6; Rare:89 | ||||
| chr8:22604554-22605076 | Common:5; Rare:190 | ||||
| chr8:22669082-22669235 | Common:2; Rare:54 | ||||
| chr8:22999753-22999990 | Common:1; Rare:57 | ||||
| chr8:23102679-23102940 | Common:1; Rare:45 | ||||
| chr8:23163998-23164142 | Rare:30 | ||||
| chr8:23457587-23457841 | Common:5; Rare:88 | ||||
| chr8:23528623-23529053 | Rare:131 |