| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:98117108-98117340 | Common:4; Rare:80 | ||||
| chr8:98944168-98944448 | Common:1; Rare:73 | ||||
| chr8:99013000-99013343 | Rare:69 | ||||
| chr8:100150564-100150709 | Rare:44 | ||||
| chr8:100310028-100310336 | Common:1; Rare:125 | ||||
| chr8:100950553-100950706 | Common:8; Rare:81 | ||||
| chr8:101205450-101205491 | Common:1; Rare:9 | ||||
| chr8:102864153-102864468 | Common:2; Rare:121 | ||||
| chr8:103298702-103298938 | Common:1; Rare:59 | ||||
| chr8:103371398-103371800 | Common:1; Rare:155; Clinvar (pathogenic):1 | ||||
| chr8:103372210-103372554 | Common:1; Rare:63 | ||||
| chr8:103415007-103415485 | Common:6; Rare:241 | ||||
| chr8:106657559-106657924 | Common:5; Rare:103 | ||||
| chr8:108248672-108248839 | Rare:72 | ||||
| chr8:108443426-108443674 | Common:4; Rare:112 |