| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238426664-238427067 | Common:6; Rare:118 | ||||
| chr2:238847919-238848245 | Rare:74 | ||||
| chr2:239309138-239309373 | Rare:51 | ||||
| chr2:239401641-239401771 | Rare:66 | ||||
| chr2:240025253-240025429 | Common:2; Rare:64; Clinvar:4; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr2:240560760-240560873 | Common:1; Rare:49 | ||||
| chr2:241096358-241096640 | Rare:58 | ||||
| chr2:241102271-241102395 | Common:2; Rare:43 | ||||
| chr2:241149464-241149573 | Common:1; Rare:32 | ||||
| chr2:241188443-241188702 | Common:2; Rare:63 | ||||
| chr2:241272769-241272970 | Rare:73 | ||||
| chr2:241315140-241315405 | Common:5; Rare:87 | ||||
| chr2:241315649-241315994 | Common:5; Rare:132 | ||||
| chr2:241508499-241508881 | Common:2; Rare:123 | ||||
| chr2:241637534-241637704 | Common:1; Rare:92 |