| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:97775751-97775917 | Common:3; Rare:78 | ||||
| chr8:98045503-98045660 | Common:2; Rare:54 | ||||
| chr8:98117114-98117333 | Common:4; Rare:74 | ||||
| chr8:99013253-99013346 | Rare:22 | ||||
| chr8:100950422-100950709 | Common:10; Rare:122 | ||||
| chr8:101204701-101204842 | Common:1; Rare:28 | ||||
| chr8:102412690-102412960 | Common:3; Rare:67 | ||||
| chr8:102864152-102864278 | Rare:57 | ||||
| chr8:103298730-103298927 | Common:1; Rare:49 | ||||
| chr8:103415063-103415469 | Common:6; Rare:213 | ||||
| chr8:107497278-107497625 | Common:2; Rare:103 | ||||
| chr8:108248683-108248872 | Rare:75 | ||||
| chr8:109334060-109334465 | Common:1; Rare:107 | ||||
| chr8:116874615-116874930 | Common:6; Rare:133; Clinvar (benign):1 | ||||
| chr8:116938422-116938471 | Common:1; Rare:16 |