| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:11853400-11853699 | Common:7; Rare:119 | ||||
| chr8:11868006-11868316 | Rare:146 | ||||
| chr8:13133243-13133572 | Common:13; Rare:88 | ||||
| chr8:13276283-13276360 | Rare:15 | ||||
| chr8:13514624-13514962 | Common:1; Rare:78 | ||||
| chr8:13566735-13566961 | Common:6; Rare:82 | ||||
| chr8:15540134-15540483 | Common:5; Rare:141; Clinvar:13; Clinvar (benign):1 | ||||
| chr8:17246589-17247063 | Common:5; Rare:198 | ||||
| chr8:17674918-17675201 | Common:5; Rare:74 | ||||
| chr8:17675239-17675266 | Rare:8 | ||||
| chr8:17676464-17676815 | Common:6; Rare:88 | ||||
| chr8:17692203-17692380 | Rare:51 | ||||
| chr8:17697450-17697737 | Common:1; Rare:63 | ||||
| chr8:17800798-17801068 | Common:3; Rare:75 | ||||
| chr8:17801075-17801344 | Common:7; Rare:101 |