| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064113-104064142 | Rare:6 | ||||
| chr12:104064435-104064570 | Rare:30 | ||||
| chr12:104138147-104138371 | Rare:53 | ||||
| chr12:104288898-104288936 | Rare:15 | ||||
| chr12:104958235-104958380 | Common:3; Rare:43 | ||||
| chr12:104986208-104986346 | Common:2; Rare:41 | ||||
| chr12:105107612-105107797 | Common:1; Rare:87 | ||||
| chr12:105236058-105236294 | Common:2; Rare:105 | ||||
| chr12:106357648-106357823 | Common:3; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106774568-106774692 | Rare:40 | ||||
| chr12:106955496-106955907 | Common:1; Rare:153 | ||||
| chr12:106987040-106987258 | Common:4; Rare:62 | ||||
| chr12:107685709-107685895 | Rare:66 | ||||
| chr12:108515054-108515280 | Common:1; Rare:63 | ||||
| chr12:108561141-108561488 | Common:4; Rare:85 |