| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:22056871-22056975 | Rare:21 | ||||
| chr8:22231970-22232053 | Rare:15 | ||||
| chr8:22245023-22245417 | Common:2; Rare:141 | ||||
| chr8:22441059-22441289 | Common:5; Rare:48 | ||||
| chr8:23164028-23164262 | Rare:46 | ||||
| chr8:23457617-23457808 | Common:2; Rare:69 | ||||
| chr8:24913448-24913773 | Common:1; Rare:78 | ||||
| chr8:26291388-26291508 | Common:1; Rare:50 | ||||
| chr8:26382971-26383123 | Common:2; Rare:70 | ||||
| chr8:26513832-26514272 | Common:2; Rare:97 | ||||
| chr8:27258367-27258550 | Rare:34 | ||||
| chr8:27258597-27258623 | Rare:2 | ||||
| chr8:27311259-27311499 | Common:6; Rare:85 | ||||
| chr8:27774274-27774580 | Common:2; Rare:64; Clinvar (benign):1 | ||||
| chr8:28092814-28093225 | Common:4; Rare:122 |