| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:130182091-130182301 | Common:2; Rare:75 | ||||
| chr2:130342127-130342242 | Rare:45 | ||||
| chr2:130342642-130342927 | Common:5; Rare:89 | ||||
| chr2:131105193-131105351 | Common:1; Rare:67 | ||||
| chr2:134918619-134918852 | Common:1; Rare:94 | ||||
| chr2:135531178-135531502 | Common:1; Rare:64 | ||||
| chr2:137964387-137964495 | Rare:19 | ||||
| chr2:144517333-144517585 | Rare:74; Clinvar:3; Clinvar (benign):4 | ||||
| chr2:144520304-144520560 | Common:4; Rare:43; Clinvar (benign):1 | ||||
| chr2:148020692-148021015 | Common:2; Rare:68 | ||||
| chr2:152717829-152717964 | Rare:56 | ||||
| chr2:152717999-152718296 | Common:1; Rare:95 | ||||
| chr2:152718481-152718637 | Rare:61 | ||||
| chr2:156332641-156332865 | Rare:67; Clinvar:3 | ||||
| chr2:159712382-159712591 | Common:2; Rare:86 |