| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17922657-17923006 | Common:4; Rare:137 | ||||
| chr8:18084784-18084864 | Common:1; Rare:40; Clinvar (benign):1 | ||||
| chr8:18084908-18084945 | Common:1; Rare:9 | ||||
| chr8:18084947-18085027 | Rare:16 | ||||
| chr8:22245026-22245455 | Common:2; Rare:153 | ||||
| chr8:22614590-22614958 | Common:4; Rare:149 | ||||
| chr8:22615815-22616044 | Common:4; Rare:90 | ||||
| chr8:23225070-23225229 | Common:1; Rare:38 | ||||
| chr8:23457625-23457771 | Common:2; Rare:57 | ||||
| chr8:26382935-26383228 | Common:3; Rare:134 | ||||
| chr8:27310243-27310543 | Common:3; Rare:47 | ||||
| chr8:27310800-27311514 | Common:9; Rare:282 | ||||
| chr8:28890204-28890416 | Rare:53 | ||||
| chr8:30083012-30083349 | Rare:116 | ||||
| chr8:30095284-30095506 | Common:2; Rare:67 |