| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr10:68407185-68407360 | Common:4; Rare:58 | ||||
| chr10:68527374-68527585 | Common:2; Rare:69 | ||||
| chr10:68901049-68901377 | Common:3; Rare:129 | ||||
| chr10:68956091-68956283 | Common:1; Rare:75 | ||||
| chr10:69087982-69088235 | Rare:53 | ||||
| chr10:69179918-69180301 | Common:2; Rare:118 | ||||
| chr10:69318609-69318950 | Common:4; Rare:100 | ||||
| chr10:69451301-69451588 | Common:2; Rare:81 | ||||
| chr10:70132740-70132906 | Rare:47 | ||||
| chr10:70146199-70146312 | Common:2; Rare:48 | ||||
| chr10:70146616-70146927 | Common:1; Rare:82 | ||||
| chr10:70170419-70170719 | Common:4; Rare:97 | ||||
| chr10:70233331-70233563 | Common:6; Rare:82; Clinvar (benign):1 | ||||
| chr10:70404103-70404543 | Common:1; Rare:138 | ||||
| chr10:71773458-71773751 | Common:4; Rare:88 |