| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49188977-49189136 | Rare:52; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49189140-49189290 | Rare:33 | ||||
| chr12:49264982-49265092 | Rare:45 | ||||
| chr12:49568098-49568220 | Common:2; Rare:42 | ||||
| chr12:49623309-49623579 | Common:1; Rare:70 | ||||
| chr12:49828380-49828530 | Common:1; Rare:57 | ||||
| chr12:49843092-49843377 | Common:1; Rare:72 | ||||
| chr12:50085291-50085384 | Common:1; Rare:22 | ||||
| chr12:50111867-50112276 | Common:2; Rare:91 | ||||
| chr12:50283475-50283664 | Common:2; Rare:59 | ||||
| chr12:50763925-50764145 | Common:1; Rare:61 | ||||
| chr12:50924470-50924739 | Common:3; Rare:78 | ||||
| chr12:51048095-51048398 | Common:2; Rare:108 | ||||
| chr12:51173061-51173261 | Rare:38 | ||||
| chr12:51238648-51238914 | Common:8; Rare:115 |