| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:925602-925725 | Not yet | Common:1; Rare:39 | 94 | ||
| chr1:1231967-1232326 | Not yet | Rare:138; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):2 | 308 | ||
| chr1:1273805-1274039 | Not yet | Rare:85 | 183 | ||
| chr1:1324580-1324859 | Not yet | Common:3; Rare:146 | 299 | ||
| chr1:1358523-1358849 | Not yet | Common:2; Rare:109 | 304 | ||
| chr1:1399182-1399595 | Not yet | Common:1; Rare:190 | 329 | ||
| chr1:1407153-1407358 | Not yet | Common:1; Rare:92 | 254 | ||
| chr1:1425581-1425896 | Not yet | Common:4; Rare:95 | 293 | ||
| chr1:1435572-1435759 | Not yet | Rare:69 | 117 | ||
| chr1:1574521-1574963 | Not yet | Common:1; Rare:199 | 342 | ||
| chr1:1615407-1615546 | Not yet | Common:1; Rare:75 | 179 | ||
| chr1:1615751-1615956 | Not yet | Common:1; Rare:67 | 147 | ||
| chr1:1658926-1659051 | Not yet | Common:2; Rare:46 | 267 | ||
| chr1:1692470-1692546 | Not yet | Common:2; Rare:13 | 88 | ||
| chr1:1724257-1724466 | Not yet | Common:3; Rare:75 | 362 |