| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:17413281-17413572 | Common:4; Rare:154 | ||||
| chr8:17692197-17692388 | Common:1; Rare:57 | ||||
| chr8:17801080-17801344 | Common:7; Rare:99 | ||||
| chr8:17910366-17910477 | Common:2; Rare:35 | ||||
| chr8:17922599-17923018 | Common:5; Rare:165 | ||||
| chr8:18084772-18085064 | Common:2; Rare:95; Clinvar (benign):1 | ||||
| chr8:19013629-19013983 | Common:5; Rare:107 | ||||
| chr8:19494471-19494806 | Common:2; Rare:64 | ||||
| chr8:19495270-19495645 | Rare:92 | ||||
| chr8:19602205-19602239 | Rare:9 | ||||
| chr8:19602440-19602519 | Common:2; Rare:34 | ||||
| chr8:19757221-19757474 | Common:3; Rare:90 | ||||
| chr8:19757866-19758020 | Common:1; Rare:28 | ||||
| chr8:19817085-19817529 | Common:8; Rare:154 | ||||
| chr8:20197184-20197412 | Common:1; Rare:102 |