| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:229921924-229922213 | Common:2; Rare:111 | ||||
| chr2:229922286-229922513 | Common:1; Rare:58 | ||||
| chr2:229923167-229923257 | Rare:21 | ||||
| chr2:231710278-231710553 | Common:2; Rare:137 | ||||
| chr2:231961639-231961748 | Rare:33; Clinvar:1 | ||||
| chr2:232550550-232550721 | Rare:65 | ||||
| chr2:237085761-237085973 | Common:2; Rare:79 | ||||
| chr2:237487141-237487298 | Common:3; Rare:42 | ||||
| chr2:237966728-237967077 | Common:4; Rare:107 | ||||
| chr2:239309171-239309373 | Rare:41 | ||||
| chr2:240025291-240025480 | Common:1; Rare:75; Clinvar:4; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr2:240456634-240456948 | Rare:85 | ||||
| chr2:241102276-241102380 | Common:2; Rare:37 | ||||
| chr2:241272794-241273030 | Rare:82 | ||||
| chr2:241315150-241315398 | Common:4; Rare:82 |