| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:232950462-232950640 | Common:2; Rare:64 | ||||
| chr1:234373314-234373554 | Common:1; Rare:117; Clinvar (benign):3 | ||||
| chr1:234373642-234373775 | Rare:51; Clinvar (benign):3 | ||||
| chr1:235128794-235129011 | Rare:81 | ||||
| chr1:235328791-235329018 | Common:1; Rare:75 | ||||
| chr1:235866904-235867152 | Common:2; Rare:68 | ||||
| chr1:236281949-236282249 | Common:6; Rare:87 | ||||
| chr1:236604466-236604645 | Common:4; Rare:52 | ||||
| chr1:236795040-236795437 | Common:6; Rare:161; Clinvar:3 | ||||
| chr1:241519684-241519950 | Common:2; Rare:83; Clinvar:8; Clinvar (benign):4; Clinvar (pathogenic):2 | ||||
| chr1:241847943-241848016 | Rare:18 | ||||
| chr1:241848094-241848266 | Common:2; Rare:32 | ||||
| chr1:243255201-243255548 | Common:1; Rare:75 | ||||
| chr1:243255776-243256078 | Rare:82; Clinvar:4 | ||||
| chr1:244451840-244452212 | Common:1; Rare:125 |