| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:51499939-51500384 | Common:1; Rare:97 | ||||
| chr3:51941867-51942347 | Common:4; Rare:133 | ||||
| chr3:51975021-51975190 | Common:1; Rare:67 | ||||
| chr3:51983062-51983306 | Common:1; Rare:50 | ||||
| chr3:51983328-51983551 | Rare:50 | ||||
| chr3:51995740-51996042 | Common:3; Rare:96 | ||||
| chr3:52154373-52154521 | Common:1; Rare:39 | ||||
| chr3:52197994-52198171 | Common:1; Rare:75 | ||||
| chr3:52239058-52239268 | Common:2; Rare:72 | ||||
| chr3:52278625-52278808 | Rare:66 | ||||
| chr3:52287727-52287859 | Common:2; Rare:49 | ||||
| chr3:52288018-52288149 | Rare:44 | ||||
| chr3:52451743-52452096 | Rare:102; Clinvar:6; Clinvar (benign):6 | ||||
| chr3:52452838-52453129 | Common:3; Rare:50 | ||||
| chr3:52453922-52454097 | Rare:46; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |