| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:49018735-49018901 | Rare:67 | ||||
| chr12:49110647-49110787 | Rare:29 | ||||
| chr12:49110840-49111058 | Rare:54 | ||||
| chr12:49131296-49131584 | Rare:115 | ||||
| chr12:49188482-49188595 | Common:1; Rare:16 | ||||
| chr12:49188979-49189290 | Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:49264781-49265092 | Common:4; Rare:111 | ||||
| chr12:49322964-49323313 | Common:3; Rare:86 | ||||
| chr12:49366774-49367021 | Common:1; Rare:64 | ||||
| chr12:49367205-49367530 | Common:1; Rare:90 | ||||
| chr12:49568104-49568216 | Common:2; Rare:37 | ||||
| chr12:49623295-49623571 | Common:1; Rare:76 | ||||
| chr12:49828387-49828575 | Common:1; Rare:69 | ||||
| chr12:49843095-49843187 | Common:1; Rare:33 | ||||
| chr12:50085077-50085364 | Common:1; Rare:73 |