| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:100150555-100150709 | Rare:48 | ||||
| chr8:100309892-100310346 | Common:1; Rare:173 | ||||
| chr8:100950418-100950580 | Common:3; Rare:56 | ||||
| chr8:100950583-100950675 | Common:8; Rare:55 | ||||
| chr8:100953278-100953496 | Common:1; Rare:48 | ||||
| chr8:101206062-101206117 | Rare:13 | ||||
| chr8:102238773-102239067 | Common:6; Rare:109; Clinvar:1; Clinvar (benign):6; Clinvar (pathogenic):2 | ||||
| chr8:102655624-102655844 | Common:1; Rare:80 | ||||
| chr8:102864079-102864532 | Common:6; Rare:179 | ||||
| chr8:103020953-103021127 | Rare:52 | ||||
| chr8:103141328-103141433 | Rare:23 | ||||
| chr8:103298619-103298938 | Common:2; Rare:77 | ||||
| chr8:103414782-103414954 | Rare:73 | ||||
| chr8:103415090-103415512 | Common:6; Rare:211 | ||||
| chr8:103500407-103500915 | Common:4; Rare:131 |