| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:34022284-34022590 | Common:3; Rare:81 | ||||
| chr12:38905584-38905710 | Common:3; Rare:34 | ||||
| chr12:38906683-38906851 | Common:1; Rare:40 | ||||
| chr12:39443379-39443552 | Rare:53; Clinvar (benign):1 | ||||
| chr12:40692288-40692586 | Common:1; Rare:90 | ||||
| chr12:42144859-42145005 | Common:3; Rare:53 | ||||
| chr12:42326006-42326232 | Common:2; Rare:76 | ||||
| chr12:42483608-42483756 | Common:1; Rare:37 | ||||
| chr12:43758696-43759021 | Common:2; Rare:94; Clinvar:2 | ||||
| chr12:43806307-43806399 | Common:1; Rare:22 | ||||
| chr12:45215601-45215874 | Rare:46 | ||||
| chr12:45215892-45216158 | Common:3; Rare:82 | ||||
| chr12:45216237-45216303 | Rare:21 | ||||
| chr12:45729539-45729934 | Common:1; Rare:115; Clinvar:1 | ||||
| chr12:45990504-45990919 | Common:2; Rare:133 |