| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:182392057-182392822 | Common:17; Rare:348; Clinvar (benign):3 | ||||
| chr1:182588928-182589106 | Common:2; Rare:34 | ||||
| chr1:182589170-182589341 | Rare:59 | ||||
| chr1:182604270-182604635 | Rare:116 | ||||
| chr1:182789513-182789834 | Common:6; Rare:203 | ||||
| chr1:182839092-182839449 | Common:3; Rare:307 | ||||
| chr1:182839532-182839778 | Common:4; Rare:200 | ||||
| chr1:182839942-182840155 | Common:4; Rare:83 | ||||
| chr1:182953510-182953879 | Common:2; Rare:90 | ||||
| chr1:183022998-183023524 | Common:17; Rare:380 | ||||
| chr1:183023810-183024420 | Common:10; Rare:331 | ||||
| chr1:183186089-183186359 | Common:8; Rare:114; Clinvar:4; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr1:183471790-183472120 | Common:3; Rare:146 | ||||
| chr1:183472205-183472585 | Common:6; Rare:285 | ||||
| chr1:183472984-183473272 | Common:2; Rare:57 |