| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:36088741-36088922 | Not yet | Common:1; Rare:67 | 170 | ||
| chr1:36397881-36398008 | Not yet | Common:2; Rare:30 | 165 | ||
| chr1:36464180-36464467 | Not yet | Common:2; Rare:87 | 334 | ||
| chr1:37474395-37474581 | Not yet | Common:1; Rare:74 | 256 | ||
| chr1:37690502-37690653 | Not yet | Common:3; Rare:44 | 239 | ||
| chr1:37692215-37692577 | Not yet | Common:4; Rare:85 | 318 | ||
| chr1:37859594-37859764 | Not yet | Common:3; Rare:56 | 270 | ||
| chr1:38873281-38873554 | Not yet | Common:3; Rare:89 | 328 | ||
| chr1:39026245-39026396 | Not yet | Common:1; Rare:40 | 205 | ||
| chr1:39738746-39738907 | Not yet | Common:2; Rare:33 | 169 | ||
| chr1:39883454-39883570 | Not yet | Common:1; Rare:48; Clinvar (pathogenic):1 | 161 | ||
| chr1:39954919-39955165 | Not yet | Common:1; Rare:63 | 236 | ||
| chr1:40040444-40040830 | Not yet | Common:3; Rare:117 | 300 | ||
| chr1:40161234-40161394 | Not yet | Common:1; Rare:42 | 229 | ||
| chr1:40257908-40258282 | Not yet | Common:4; Rare:101; Clinvar:7; Clinvar (benign):1 | 302 |