| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:70669166-70669391 | Common:2; Rare:66 | ||||
| chr8:71843753-71844284 | Rare:190 | ||||
| chr8:73294413-73294605 | Common:1; Rare:70 | ||||
| chr8:85177025-85177163 | Common:1; Rare:35 | ||||
| chr8:86514356-86514443 | Common:1; Rare:22 | ||||
| chr8:89757626-89757856 | Common:1; Rare:88 | ||||
| chr8:91040805-91040994 | Common:2; Rare:62 | ||||
| chr8:91070023-91070352 | Common:1; Rare:116 | ||||
| chr8:96261594-96261933 | Common:5; Rare:104 | ||||
| chr8:97868990-97869124 | Rare:20 | ||||
| chr8:98045532-98045663 | Common:1; Rare:44 | ||||
| chr8:98117144-98117325 | Common:2; Rare:61 | ||||
| chr8:102864154-102864196 | Rare:26 | ||||
| chr8:103298723-103298898 | Common:1; Rare:41 | ||||
| chr8:103371705-103371801 | Rare:38; Clinvar (pathogenic):1 |