| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48716639-48717008 | Common:4; Rare:110 | ||||
| chr12:48814673-48814861 | Rare:33 | ||||
| chr12:49018744-49018968 | Common:1; Rare:88 | ||||
| chr12:49131341-49131614 | Common:2; Rare:106 | ||||
| chr12:49188975-49189350 | Rare:96; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49367203-49367582 | Common:1; Rare:101 | ||||
| chr12:49568110-49568221 | Common:2; Rare:37 | ||||
| chr12:49623276-49623575 | Common:1; Rare:86 | ||||
| chr12:49828387-49828543 | Common:1; Rare:57 | ||||
| chr12:50283478-50283662 | Common:2; Rare:58 | ||||
| chr12:50400780-50400982 | Rare:61 | ||||
| chr12:50763937-50764334 | Common:1; Rare:105 | ||||
| chr12:50924553-50924719 | Common:1; Rare:32 | ||||
| chr12:51048233-51048368 | Common:1; Rare:63 | ||||
| chr12:51173034-51173291 | Rare:50 |