| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr2:240025225-240025452 | Common:2; Rare:81; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr2:240136243-240136382 | Rare:55 | ||||
| chr2:240560760-240560873 | Common:1; Rare:49 | ||||
| chr2:240561054-240561290 | Common:3; Rare:102 | ||||
| chr2:240586608-240586859 | Common:3; Rare:80 | ||||
| chr2:240891995-240892113 | Common:2; Rare:21 | ||||
| chr2:240896043-240896336 | Common:4; Rare:58 | ||||
| chr2:240896813-240897034 | Common:3; Rare:46 | ||||
| chr2:241102255-241102420 | Common:2; Rare:56 | ||||
| chr2:241149429-241149621 | Common:3; Rare:62 | ||||
| chr2:241230757-241231203 | Common:1; Rare:110 | ||||
| chr2:241239600-241240121 | Common:2; Rare:165 | ||||
| chr2:241248010-241248349 | Common:1; Rare:90 | ||||
| chr2:241272770-241272920 | Rare:55 | ||||
| chr2:241315114-241315406 | Common:5; Rare:99 |