| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:233854482-233854724 | Common:5; Rare:68 | ||||
| chr2:236507423-236507653 | Common:6; Rare:79 | ||||
| chr2:237085807-237085951 | Common:1; Rare:58 | ||||
| chr2:237487197-237487277 | Common:1; Rare:20 | ||||
| chr2:237966728-237967078 | Common:4; Rare:108 | ||||
| chr2:238203583-238203797 | Common:3; Rare:88 | ||||
| chr2:240025253-240025452 | Common:2; Rare:72; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240136253-240136411 | Common:1; Rare:71 | ||||
| chr2:241102271-241102360 | Common:2; Rare:35 | ||||
| chr2:241149464-241149639 | Common:2; Rare:53 | ||||
| chr2:241272802-241272964 | Rare:66 | ||||
| chr2:241315116-241315409 | Common:5; Rare:98 | ||||
| chr2:241315649-241315994 | Common:5; Rare:132 | ||||
| chr2:241508573-241508901 | Common:1; Rare:104 | ||||
| chr2:241637544-241637711 | Common:1; Rare:92 |