| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr19:27793370-27793498 | Not yet | Common:1; Rare:32 | 229 | ||
| chr19:27793681-27794027 | Not yet | Rare:89 | 295 | ||
| chr19:36797323-36797534 | Not yet | Rare:40 | 359 | ||
| chr19:41500618-41500790 | Not yet | Common:1; Rare:32 | 364 | ||
| chr19:41531561-41531708 | Not yet | Common:1; Rare:35 | 281 | ||
| chr19:42396907-42397184 | Not yet | Common:1; Rare:66 | 258 | ||
| chr19:46860839-46861114 | Not yet | Common:3; Rare:88 | 204 | ||
| chr19:48873016-48873259 | Not yet | Common:2; Rare:43 | 401 | ||
| chr19:48966390-48966673 | Not yet | Rare:91; Clinvar:1 | 393 | ||
| chr19:49009806-49010064 | Not yet | Common:1; Rare:99 | 272 | ||
| chr19:49090328-49090508 | Not yet | Rare:44 | 268 | ||
| chr19:52923411-52923549 | Not yet | Common:3; Rare:54 | 126 | ||
| chr2:19933425-19933721 | Not yet | Common:4; Rare:59; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | 395 | ||
| chr2:55282204-55282368 | Not yet | Common:5; Rare:57 | 136 | ||
| chr2:55989489-55989666 | Not yet | Common:3; Rare:31 | 313 |