| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94949316-94949604 | Common:3; Rare:82 | ||||
| chr8:96261574-96261943 | Common:5; Rare:120 | ||||
| chr8:97644663-97644881 | Common:1; Rare:77 | ||||
| chr8:98045389-98045619 | Common:3; Rare:73 | ||||
| chr8:98117104-98117353 | Common:4; Rare:85 | ||||
| chr8:99013208-99013344 | Rare:31 | ||||
| chr8:100150565-100150670 | Rare:32 | ||||
| chr8:101204701-101204849 | Common:1; Rare:29 | ||||
| chr8:102864158-102864271 | Rare:52 | ||||
| chr8:103298709-103298901 | Common:1; Rare:47 | ||||
| chr8:103371396-103371803 | Common:1; Rare:157; Clinvar (pathogenic):1 | ||||
| chr8:103415090-103415455 | Common:6; Rare:188 | ||||
| chr8:109334060-109334449 | Common:1; Rare:105 | ||||
| chr8:116755783-116755943 | Common:1; Rare:74 | ||||
| chr8:118110300-118110479 | Rare:42; Clinvar:1 |