| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:13133193-13133606 | Common:14; Rare:124 | ||||
| chr8:13566743-13566910 | Common:6; Rare:60 | ||||
| chr8:16192619-16192936 | Common:5; Rare:81 | ||||
| chr8:17246589-17247084 | Common:5; Rare:204 | ||||
| chr8:17801080-17801346 | Common:7; Rare:99 | ||||
| chr8:17922606-17922929 | Common:4; Rare:120 | ||||
| chr8:17922933-17923045 | Common:1; Rare:49 | ||||
| chr8:17923211-17923342 | Rare:44 | ||||
| chr8:18084820-18085038 | Common:2; Rare:60; Clinvar (benign):1 | ||||
| chr8:19313563-19313746 | Common:3; Rare:56 | ||||
| chr8:19313923-19314001 | Rare:33 | ||||
| chr8:19817074-19817666 | Common:8; Rare:217 | ||||
| chr8:21919561-21919773 | Common:2; Rare:86 | ||||
| chr8:22141854-22141978 | Common:2; Rare:38 | ||||
| chr8:22245024-22245452 | Common:2; Rare:153 |