| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:238239997-238240317 | Common:2; Rare:116 | ||||
| chr2:238240598-238241534 | Common:5; Rare:243 | ||||
| chr2:238288750-238288978 | Rare:88 | ||||
| chr2:238320213-238320532 | Common:1; Rare:98 | ||||
| chr2:238426229-238426379 | Common:2; Rare:40 | ||||
| chr2:238426820-238427067 | Common:2; Rare:90 | ||||
| chr2:238848105-238848670 | Rare:220; Clinvar (pathogenic):3 | ||||
| chr2:239401634-239401805 | Rare:91 | ||||
| chr2:240025299-240025589 | Common:2; Rare:115; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr2:240136238-240136463 | Common:2; Rare:97 | ||||
| chr2:240435190-240435363 | Common:1; Rare:73 | ||||
| chr2:240435612-240435714 | Rare:38 | ||||
| chr2:240560670-240560950 | Common:3; Rare:141 | ||||
| chr2:240561007-240561326 | Common:4; Rare:154 | ||||
| chr2:240567909-240569011 | Common:5; Rare:376 |