| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:61017171-61017794 | Common:5; Rare:194; Clinvar:7; Clinvar (benign):2 | ||||
| chr2:61065588-61066006 | Common:4; Rare:129 | ||||
| chr2:61144901-61145185 | Common:3; Rare:95 | ||||
| chr2:61470651-61470991 | Rare:112 | ||||
| chr2:61471252-61471337 | Common:1; Rare:24 | ||||
| chr2:61537566-61537866 | Common:2; Rare:88 | ||||
| chr2:61853992-61854228 | Common:2; Rare:97; Clinvar:1; Clinvar (benign):1 | ||||
| chr2:61888448-61888714 | Common:1; Rare:117 | ||||
| chr2:61905607-61905699 | Rare:47 | ||||
| chr2:62506131-62506297 | Common:1; Rare:65 | ||||
| chr2:63044814-63045069 | Rare:36 | ||||
| chr2:63588218-63588566 | Common:1; Rare:106; Clinvar:6 | ||||
| chr2:63588693-63589046 | Rare:112 | ||||
| chr2:63840812-63841212 | Common:3; Rare:114 | ||||
| chr2:63841648-63841921 | Common:2; Rare:96 |