| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:57200525-57200786 | Common:1; Rare:55 | ||||
| chr12:57201481-57201850 | Common:2; Rare:89 | ||||
| chr12:57229603-57229753 | Common:1; Rare:74 | ||||
| chr12:57230014-57230212 | Rare:41 | ||||
| chr12:57430766-57431087 | Common:1; Rare:87 | ||||
| chr12:57477812-57478130 | Rare:69 | ||||
| chr12:57520501-57520729 | Common:1; Rare:68 | ||||
| chr12:57522642-57522905 | Common:3; Rare:112 | ||||
| chr12:57526443-57526674 | Common:2; Rare:62 | ||||
| chr12:57610066-57610304 | Common:2; Rare:65 | ||||
| chr12:57694207-57694291 | Rare:18 | ||||
| chr12:57716088-57716741 | Common:4; Rare:170 | ||||
| chr12:57746082-57746245 | Rare:47 | ||||
| chr12:57752209-57752742 | Common:1; Rare:140; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:57772079-57772251 | Rare:60 |