| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120116606-120116938 | Common:5; Rare:90 | ||||
| chr12:120194690-120194798 | Rare:39 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120249528-120249720 | Rare:26 | ||||
| chr12:120250106-120250217 | Common:1; Rare:21 | ||||
| chr12:120437853-120438229 | Common:2; Rare:141; Clinvar (benign):2 | ||||
| chr12:120446346-120446483 | Common:1; Rare:61 | ||||
| chr12:120469538-120469873 | Common:2; Rare:117 | ||||
| chr12:120495859-120496239 | Common:7; Rare:128 | ||||
| chr12:120529094-120529263 | Common:2; Rare:62 | ||||
| chr12:120534308-120534363 | Rare:23 | ||||
| chr12:120566648-120566932 | Common:3; Rare:69 | ||||
| chr12:120575554-120575912 | Common:3; Rare:92 | ||||
| chr12:120581348-120581588 | Common:1; Rare:83 | ||||
| chr12:121209937-121210152 | Common:5; Rare:69 |