| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:1615727-1615926 | Common:3; Rare:128 | ||||
| chr1:1658931-1659096 | Common:4; Rare:107 | ||||
| chr1:1724246-1724481 | Common:6; Rare:158 | ||||
| chr1:1778384-1778566 | Common:4; Rare:118 | ||||
| chr1:1778777-1779013 | Common:1; Rare:105 | ||||
| chr1:1890544-1890878 | Common:4; Rare:186 | ||||
| chr1:1890903-1891215 | Rare:210 | ||||
| chr1:1891310-1891600 | Common:6; Rare:91 | ||||
| chr1:2050109-2050562 | Common:4; Rare:326 | ||||
| chr1:2134739-2135018 | Common:2; Rare:137 | ||||
| chr1:2194691-2194840 | Rare:93 | ||||
| chr1:2207660-2208060 | Common:12; Rare:206 | ||||
| chr1:2231920-2232300 | Common:6; Rare:189 | ||||
| chr1:2391518-2391919 | Common:2; Rare:147 | ||||
| chr1:2412500-2412850 | Common:2; Rare:286; Clinvar:4; Clinvar (pathogenic):2 |