| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:37859586-37859764 | Not yet | Common:3; Rare:58 | 279 | ||
| chr1:37989981-37990105 | Not yet | Rare:47 | 195 | ||
| chr1:38005495-38005766 | Not yet | Common:1; Rare:68 | 183 | ||
| chr1:38012443-38012799 | Not yet | Common:1; Rare:106 | 356 | ||
| chr1:38859692-38859940 | Not yet | Rare:95 | 326 | ||
| chr1:38873306-38873551 | Not yet | Common:3; Rare:84 | 267 | ||
| chr1:39026237-39026398 | Not yet | Common:1; Rare:43 | 216 | ||
| chr1:39883447-39883570 | Not yet | Common:1; Rare:51; Clinvar (pathogenic):1 | 166 | ||
| chr1:39955004-39955193 | Not yet | Common:1; Rare:50 | 150 | ||
| chr1:40040089-40040240 | Not yet | Common:1; Rare:27 | 270 | ||
| chr1:40040419-40040799 | Not yet | Common:3; Rare:120 | 289 | ||
| chr1:40161231-40161402 | Not yet | Common:1; Rare:47 | 232 | ||
| chr1:40257908-40258292 | Not yet | Common:4; Rare:106; Clinvar:7; Clinvar (benign):1 | 304 | ||
| chr1:40508674-40508773 | Not yet | Common:3; Rare:27 | 109 | ||
| chr1:40691495-40691810 | Not yet | Common:3; Rare:155 | 288 |