| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:96645220-96645381 | Common:1; Rare:44 | ||||
| chr8:97277891-97277977 | Rare:35 | ||||
| chr8:97775724-97776004 | Common:4; Rare:142; Clinvar (benign):1 | ||||
| chr8:97868987-97869146 | Rare:30 | ||||
| chr8:98045348-98045676 | Common:4; Rare:98 | ||||
| chr8:98117120-98117333 | Common:4; Rare:69 | ||||
| chr8:98825630-98825890 | Rare:84 | ||||
| chr8:99012991-99013368 | Rare:78; Clinvar:1 | ||||
| chr8:100150564-100150706 | Rare:44 | ||||
| chr8:100309904-100310284 | Common:1; Rare:136 | ||||
| chr8:100709133-100709571 | Common:6; Rare:115 | ||||
| chr8:100951265-100951460 | Common:2; Rare:71 | ||||
| chr8:100953326-100953455 | Common:1; Rare:29 | ||||
| chr8:101492237-101492485 | Common:2; Rare:42 | ||||
| chr8:101492514-101492575 | Rare:20 |