| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:32755095-32755343 | Common:1; Rare:71; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr12:32755827-32756021 | Rare:72 | ||||
| chr12:34022284-34022502 | Common:2; Rare:54 | ||||
| chr12:38905449-38905676 | Common:4; Rare:66 | ||||
| chr12:42237594-42237898 | Common:1; Rare:81 | ||||
| chr12:42238148-42238409 | Common:1; Rare:77 | ||||
| chr12:42326002-42326226 | Common:1; Rare:74 | ||||
| chr12:43758735-43759021 | Common:2; Rare:81; Clinvar:2 | ||||
| chr12:43806306-43806613 | Common:3; Rare:85 | ||||
| chr12:43836027-43836081 | Common:1; Rare:13 | ||||
| chr12:45215350-45215865 | Common:1; Rare:97 | ||||
| chr12:45215909-45216388 | Common:3; Rare:154 | ||||
| chr12:45729539-45729749 | Rare:62 | ||||
| chr12:45990382-45990501 | Rare:37 | ||||
| chr12:45990504-45990926 | Common:2; Rare:136 |