| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:209579415-209579731 | Common:1; Rare:57 | ||||
| chr2:210002525-210002675 | Common:4; Rare:61 | ||||
| chr2:210476675-210476862 | Rare:60 | ||||
| chr2:212538542-212538893 | Common:1; Rare:107 | ||||
| chr2:213284238-213284483 | Rare:79 | ||||
| chr2:215311888-215312115 | Common:6; Rare:90 | ||||
| chr2:215436030-215436287 | Common:2; Rare:83 | ||||
| chr2:216081756-216081935 | Common:1; Rare:62 | ||||
| chr2:216412280-216412492 | Common:1; Rare:47 | ||||
| chr2:216412664-216412775 | Rare:13 | ||||
| chr2:216498754-216498896 | Common:4; Rare:63 | ||||
| chr2:216694633-216694656 | Rare:5 | ||||
| chr2:218216947-218217226 | Common:2; Rare:97 | ||||
| chr2:218270098-218270538 | Common:5; Rare:136; Clinvar:3; Clinvar (benign):1 | ||||
| chr2:218292479-218292671 | Common:1; Rare:57 |