| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:97643844-97644327 | Common:9; Rare:124 | ||||
| chr8:97644715-97644896 | Common:1; Rare:57 | ||||
| chr8:97775704-97776084 | Common:6; Rare:183; Clinvar (benign):1 | ||||
| chr8:97868987-97869146 | Rare:30 | ||||
| chr8:98045370-98045679 | Common:4; Rare:95 | ||||
| chr8:98046109-98046166 | Common:2; Rare:10 | ||||
| chr8:98064504-98064604 | Rare:29 | ||||
| chr8:98117061-98117361 | Common:4; Rare:101 | ||||
| chr8:98294133-98294430 | Common:2; Rare:81 | ||||
| chr8:98602216-98602409 | Common:1; Rare:32 | ||||
| chr8:98942562-98942638 | Rare:14 | ||||
| chr8:99012518-99012796 | Rare:53 | ||||
| chr8:99012977-99013143 | Rare:35 | ||||
| chr8:99013190-99013464 | Rare:51; Clinvar:1 | ||||
| chr8:99893186-99893363 | Rare:36 |