| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:102104275-102104734 | Common:8; Rare:107 | ||||
| chr2:102736817-102736965 | Common:1; Rare:74 | ||||
| chr2:105037872-105038195 | Common:4; Rare:117 | ||||
| chr2:105329667-105329835 | Common:2; Rare:53 | ||||
| chr2:105337233-105337578 | Common:5; Rare:116 | ||||
| chr2:105396730-105397179 | Common:9; Rare:107 | ||||
| chr2:105397455-105397762 | Common:3; Rare:59 | ||||
| chr2:105398346-105399116 | Common:4; Rare:186 | ||||
| chr2:108449108-108449267 | Rare:63 | ||||
| chr2:108475383-108475590 | Rare:42 | ||||
| chr2:108533895-108533973 | Rare:26 | ||||
| chr2:108534148-108534541 | Common:8; Rare:153 | ||||
| chr2:108534549-108534585 | Rare:3 | ||||
| chr2:108719362-108719655 | Common:3; Rare:127; Clinvar (benign):2 | ||||
| chr2:109129024-109129166 | Rare:58 |