| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238203565-238203791 | Common:5; Rare:87 | ||||
| chr2:238426893-238427067 | Common:1; Rare:65 | ||||
| chr2:239401641-239401777 | Rare:70 | ||||
| chr2:240025225-240025583 | Common:4; Rare:135; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240560760-240560873 | Common:1; Rare:49 | ||||
| chr2:240561087-240561313 | Common:4; Rare:91 | ||||
| chr2:241102270-241102346 | Common:2; Rare:31 | ||||
| chr2:241149450-241149640 | Common:2; Rare:58 | ||||
| chr2:241236735-241237002 | Common:6; Rare:77 | ||||
| chr2:241272782-241272968 | Rare:71 | ||||
| chr2:241315109-241315327 | Common:4; Rare:79 | ||||
| chr2:241315633-241315994 | Common:5; Rare:138 | ||||
| chr2:241508557-241508864 | Common:1; Rare:96 | ||||
| chr2:241637534-241637704 | Common:1; Rare:92 | ||||
| chr2:241686785-241686992 | Rare:58 |