| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:79935188-79935349 | Rare:58 | ||||
| chr12:82358375-82358554 | Rare:74 | ||||
| chr12:89524737-89524869 | Common:1; Rare:26 | ||||
| chr12:89708779-89709004 | Rare:91 | ||||
| chr12:91182656-91182731 | Rare:11 | ||||
| chr12:98599751-98600098 | Common:2; Rare:120; Clinvar:2 | ||||
| chr12:98601172-98601449 | Rare:79; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:102120062-102120230 | Rare:64 | ||||
| chr12:103930336-103930533 | Common:4; Rare:89 | ||||
| chr12:103930542-103930554 | Rare:5 | ||||
| chr12:103965727-103965927 | Common:2; Rare:49 | ||||
| chr12:106955648-106955952 | Rare:108 | ||||
| chr12:109477293-109477436 | Common:3; Rare:49 | ||||
| chr12:109573483-109573841 | Common:3; Rare:101; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109880426-109880658 | Common:1; Rare:65 |