| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr1:21345463-21345677 | Not yet | Common:2; Rare:82 | 131 | ||
| chr1:21622549-21622711 | Not yet | Common:3; Rare:53 | 88 | ||
| chr1:21782977-21783182 | Not yet | Common:1; Rare:69 | 148 | ||
| chr1:23019277-23019635 | Not yet | Rare:126 | 128 | ||
| chr1:23019809-23019821 | Not yet | Rare:1 | 11 | ||
| chr1:23077001-23077353 | Not yet | Common:1; Rare:71 | 229 | ||
| chr1:23194795-23194965 | Not yet | Common:1; Rare:39 | 136 | ||
| chr1:23344180-23344438 | Not yet | Common:2; Rare:99 | 170 | ||
| chr1:23368161-23368494 | Not yet | Common:1; Rare:100 | 171 | ||
| chr1:23368883-23369241 | Not yet | Common:3; Rare:103 | 149 | ||
| chr1:23558909-23559159 | Not yet | Common:5; Rare:126 | 162 | ||
| chr1:23559311-23559648 | Not yet | Common:1; Rare:148 | 186 | ||
| chr1:23778238-23778451 | Not yet | Common:6; Rare:109 | 173 | ||
| chr1:23799516-23799793 | Not yet | Rare:50 | 207 | ||
| chr1:23825401-23825725 | Not yet | Common:3; Rare:77; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | 208 |