| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:224929251-224930432 | Common:38; Rare:1266 | ||||
| chr1:225427416-225427816 | Common:2; Rare:103 | ||||
| chr1:225427968-225428414 | Common:21; Rare:845; Clinvar:24; Clinvar (benign):15 | ||||
| chr1:225428573-225428973 | Common:11; Rare:235 | ||||
| chr1:225429174-225429574 | Common:4; Rare:89 | ||||
| chr1:225652990-225653350 | Common:2; Rare:141 | ||||
| chr1:225777166-225777566 | Common:2; Rare:108 | ||||
| chr1:225777552-225777994 | Common:17; Rare:519 | ||||
| chr1:225778062-225778660 | Common:11; Rare:289 | ||||
| chr1:225809848-225810599 | Common:19; Rare:307 | ||||
| chr1:225881560-225881980 | Common:14; Rare:258 | ||||
| chr1:225882190-225882551 | Common:9; Rare:360 | ||||
| chr1:225882660-225883090 | Common:19; Rare:177 | ||||
| chr1:225923044-225923776 | Common:6; Rare:408; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
| chr1:225923839-225924657 | Common:67; Rare:979 |