| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:237085815-237085951 | Common:1; Rare:55 | ||||
| chr2:237966728-237967074 | Common:3; Rare:107 | ||||
| chr2:238060738-238061110 | Common:6; Rare:117 | ||||
| chr2:238203616-238203821 | Common:3; Rare:89 | ||||
| chr2:240025253-240025519 | Common:3; Rare:108; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136250-240136423 | Common:1; Rare:76 | ||||
| chr2:240560766-240560928 | Common:2; Rare:79 | ||||
| chr2:241102265-241102508 | Common:2; Rare:74 | ||||
| chr2:241149445-241149638 | Common:2; Rare:60 | ||||
| chr2:241315109-241315333 | Common:4; Rare:81 | ||||
| chr2:241315644-241315987 | Common:5; Rare:135 | ||||
| chr2:241637544-241637714 | Common:1; Rare:94 | ||||
| chr2:241686771-241686973 | Rare:65 | ||||
| chr2:241701879-241702065 | Common:1; Rare:77 | ||||
| chr20:348165-348271 | Common:1; Rare:24 |