| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:46372740-46372995 | Rare:104 | ||||
| chr12:47706007-47706124 | Rare:46 | ||||
| chr12:48716727-48717017 | Common:4; Rare:79 | ||||
| chr12:49188986-49189296 | Rare:86; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:51048119-51048350 | Common:1; Rare:78 | ||||
| chr12:54259534-54259751 | Rare:38 | ||||
| chr12:55716021-55716169 | Common:1; Rare:71 | ||||
| chr12:55728961-55729302 | Rare:70 | ||||
| chr12:55829528-55829787 | Rare:84 | ||||
| chr12:56315905-56316227 | Common:1; Rare:76 | ||||
| chr12:56449397-56449478 | Rare:22 | ||||
| chr12:57111339-57111463 | Rare:29 | ||||
| chr12:68610733-68610942 | Rare:90 | ||||
| chr12:68686843-68687001 | Common:3; Rare:41 | ||||
| chr12:76879017-76879204 | Rare:60 |