| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:55773291-55773531 | Common:3; Rare:85 | ||||
| chr8:56074382-56074617 | Common:4; Rare:112 | ||||
| chr8:58570695-58570919 | Common:1; Rare:40 | ||||
| chr8:59119216-59119270 | Rare:18 | ||||
| chr8:60516781-60517253 | Common:3; Rare:155 | ||||
| chr8:61714094-61714341 | Common:1; Rare:68 | ||||
| chr8:61714352-61714447 | Common:2; Rare:30 | ||||
| chr8:63038718-63038920 | Common:3; Rare:80 | ||||
| chr8:63085893-63086167 | Common:3; Rare:76; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr8:63168429-63168673 | Common:2; Rare:86 | ||||
| chr8:64798539-64798892 | Common:2; Rare:106; Clinvar:8; Clinvar (benign):1 | ||||
| chr8:66126870-66127151 | Common:1; Rare:58 | ||||
| chr8:66428996-66429139 | Rare:42 | ||||
| chr8:66430037-66430311 | Rare:91 | ||||
| chr8:66432351-66432526 | Common:2; Rare:43 |