| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238426662-238427067 | Common:6; Rare:118 | ||||
| chr2:238847919-238848224 | Rare:68 | ||||
| chr2:238848474-238848503 | Rare:6 | ||||
| chr2:239401641-239401764 | Rare:60 | ||||
| chr2:240025225-240025488 | Common:3; Rare:95; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560766-240560820 | Rare:21 | ||||
| chr2:240561052-240561326 | Common:4; Rare:120 | ||||
| chr2:240586598-240586859 | Common:3; Rare:86 | ||||
| chr2:240998233-240998376 | Rare:28 | ||||
| chr2:241102279-241102512 | Common:2; Rare:67 | ||||
| chr2:241248242-241248434 | Rare:49 | ||||
| chr2:241255049-241255567 | Common:1; Rare:117 | ||||
| chr2:241256383-241256779 | Common:2; Rare:94 | ||||
| chr2:241272774-241273016 | Rare:83 | ||||
| chr2:241315102-241315420 | Common:5; Rare:112 |