| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:9151537-9151696 | Common:1; Rare:47 | ||||
| chr8:10730429-10730750 | Common:3; Rare:101 | ||||
| chr8:10839789-10840057 | Common:1; Rare:96 | ||||
| chr8:11201812-11202034 | Common:1; Rare:64 | ||||
| chr8:11284741-11284861 | Common:2; Rare:54 | ||||
| chr8:11802422-11802931 | Common:7; Rare:286 | ||||
| chr8:11867990-11868267 | Common:1; Rare:127 | ||||
| chr8:13566827-13566905 | Common:3; Rare:27 | ||||
| chr8:17246568-17247109 | Common:5; Rare:217 | ||||
| chr8:17692197-17692370 | Rare:49 | ||||
| chr8:17801080-17801349 | Common:7; Rare:101 | ||||
| chr8:17922597-17922971 | Common:4; Rare:147 | ||||
| chr8:18084779-18084864 | Common:1; Rare:42; Clinvar (benign):1 | ||||
| chr8:18084910-18085028 | Common:1; Rare:26 | ||||
| chr8:18854350-18854466 | Rare:21 |