| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:19013637-19013976 | Common:5; Rare:96 | ||||
| chr8:19817049-19817529 | Common:8; Rare:170 | ||||
| chr8:20303929-20304077 | Common:2; Rare:54 | ||||
| chr8:21919486-21919783 | Common:2; Rare:118 | ||||
| chr8:22089156-22089211 | Rare:21 | ||||
| chr8:22231951-22232099 | Common:1; Rare:36 | ||||
| chr8:22245023-22245459 | Common:2; Rare:156 | ||||
| chr8:22440972-22441305 | Common:6; Rare:83 | ||||
| chr8:22579018-22579169 | Common:1; Rare:35 | ||||
| chr8:22585119-22585399 | Common:1; Rare:88 | ||||
| chr8:22604527-22604820 | Common:1; Rare:111 | ||||
| chr8:23224883-23225261 | Common:2; Rare:110 | ||||
| chr8:23457605-23457778 | Common:3; Rare:67 | ||||
| chr8:24956067-24956191 | Rare:40; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr8:25457370-25457427 | Rare:5 |