| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:94895704-94895816 | Common:1; Rare:26 | ||||
| chr8:94949357-94949567 | Common:2; Rare:62 | ||||
| chr8:95269287-95269605 | Common:6; Rare:87 | ||||
| chr8:96235503-96235652 | Common:1; Rare:78; Clinvar (benign):2 | ||||
| chr8:96261566-96261965 | Common:6; Rare:135 | ||||
| chr8:96493743-96493852 | Rare:38 | ||||
| chr8:96494054-96494331 | Common:3; Rare:94 | ||||
| chr8:97277876-97278098 | Rare:81 | ||||
| chr8:97775724-97776053 | Common:5; Rare:163; Clinvar (benign):1 | ||||
| chr8:98045333-98045666 | Common:3; Rare:99 | ||||
| chr8:98117076-98117330 | Common:3; Rare:91 | ||||
| chr8:99013000-99013377 | Rare:77; Clinvar:1 | ||||
| chr8:100150559-100150709 | Rare:45 | ||||
| chr8:100309876-100310315 | Common:1; Rare:162 | ||||
| chr8:100709108-100709493 | Common:4; Rare:105 |