| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:42326006-42326229 | Common:2; Rare:74 | ||||
| chr12:43758753-43759007 | Common:2; Rare:72; Clinvar:2 | ||||
| chr12:45215980-45216184 | Common:1; Rare:67 | ||||
| chr12:46268593-46268701 | Rare:27 | ||||
| chr12:46269137-46269177 | Rare:9 | ||||
| chr12:46371304-46371559 | Common:2; Rare:118 | ||||
| chr12:46372635-46372963 | Rare:136 | ||||
| chr12:47079486-47079629 | Common:1; Rare:32 | ||||
| chr12:47705970-47706088 | Rare:55 | ||||
| chr12:47758801-47758975 | Common:1; Rare:34 | ||||
| chr12:47819864-47820123 | Common:2; Rare:62 | ||||
| chr12:48105834-48105952 | Rare:32 | ||||
| chr12:48106031-48106104 | Rare:22 | ||||
| chr12:48106141-48106196 | Common:1; Rare:21 | ||||
| chr12:48716631-48717008 | Common:4; Rare:111 |