| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:18084797-18084864 | Common:1; Rare:30; Clinvar (benign):1 | ||||
| chr8:18084931-18085003 | Rare:17 | ||||
| chr8:19602205-19602271 | Rare:19 | ||||
| chr8:19817336-19817515 | Common:4; Rare:72 | ||||
| chr8:21913688-21913854 | Rare:47 | ||||
| chr8:22245026-22245182 | Common:1; Rare:76 | ||||
| chr8:22604621-22604802 | Common:1; Rare:71 | ||||
| chr8:23457624-23457771 | Common:2; Rare:58 | ||||
| chr8:23528711-23529057 | Rare:108 | ||||
| chr8:26382928-26383123 | Common:2; Rare:90 | ||||
| chr8:26390233-26390450 | Common:1; Rare:38 | ||||
| chr8:26513874-26514029 | Common:1; Rare:27 | ||||
| chr8:27491016-27491227 | Common:3; Rare:80 | ||||
| chr8:27772569-27772752 | Common:6; Rare:61 | ||||
| chr8:28889909-28890409 | Rare:133 |