| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:74120562-74120588 | Rare:8 | ||||
| chr2:74377437-74377690 | Common:1; Rare:65 | ||||
| chr2:74504542-74504810 | Rare:51 | ||||
| chr2:74573763-74574091 | Common:3; Rare:42 | ||||
| chr2:74917855-74918120 | Common:4; Rare:46 | ||||
| chr2:74918144-74918443 | Common:1; Rare:64 | ||||
| chr2:75516326-75516644 | Common:1; Rare:52 | ||||
| chr2:75872356-75872455 | Rare:25 | ||||
| chr2:78203394-78203536 | Common:1; Rare:26 | ||||
| chr2:78540981-78541251 | Common:1; Rare:43 | ||||
| chr2:78541822-78542092 | Common:1; Rare:74 | ||||
| chr2:79393853-79394064 | Common:1; Rare:47 | ||||
| chr2:81481397-81481823 | Common:8; Rare:108 | ||||
| chr2:81482114-81482301 | Rare:22 | ||||
| chr2:84449739-84449975 | Common:2; Rare:58; Clinvar:1; Clinvar (benign):1 |