| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:51025762-51026012 | Common:1; Rare:55 | ||||
| chr12:51026073-51026650 | Common:7; Rare:184; Clinvar:3; Clinvar (benign):2 | ||||
| chr12:51028211-51028405 | Rare:45 | ||||
| chr12:51047822-51048021 | Common:2; Rare:37 | ||||
| chr12:51048070-51048407 | Common:2; Rare:117 | ||||
| chr12:51082914-51083076 | Rare:31 | ||||
| chr12:51083191-51083267 | Rare:20 | ||||
| chr12:51083278-51083786 | Common:1; Rare:173 | ||||
| chr12:51172148-51172326 | Rare:27 | ||||
| chr12:51172341-51172392 | Rare:9 | ||||
| chr12:51172722-51172938 | Common:3; Rare:46 | ||||
| chr12:51173061-51173341 | Rare:56 | ||||
| chr12:51217238-51217462 | Common:1; Rare:63 | ||||
| chr12:51217468-51217609 | Common:1; Rare:21 | ||||
| chr12:51217614-51217829 | Common:1; Rare:53 |