| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:232776553-232776603 | Rare:8 | ||||
| chr2:233854472-233854720 | Common:5; Rare:71 | ||||
| chr2:237085761-237085951 | Common:2; Rare:69 | ||||
| chr2:237966728-237967083 | Common:4; Rare:110 | ||||
| chr2:238203591-238203803 | Common:3; Rare:91 | ||||
| chr2:238426893-238427067 | Common:1; Rare:65 | ||||
| chr2:239401641-239401758 | Rare:57 | ||||
| chr2:240025291-240025455 | Common:1; Rare:66; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:241102269-241102500 | Common:2; Rare:71 | ||||
| chr2:241149450-241149564 | Common:1; Rare:33 | ||||
| chr2:241242640-241242806 | Common:1; Rare:39 | ||||
| chr2:241272773-241273008 | Rare:80 | ||||
| chr2:241315122-241315405 | Common:5; Rare:92 | ||||
| chr2:241315646-241315989 | Common:5; Rare:133 | ||||
| chr2:241509337-241509519 | Rare:41 |