| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:53466987-53467293 | Common:1; Rare:74 | ||||
| chr12:53468020-53468045 | Rare:6 | ||||
| chr12:53501209-53501381 | Rare:41 | ||||
| chr12:53501537-53501596 | Rare:11 | ||||
| chr12:53626333-53626557 | Common:3; Rare:56 | ||||
| chr12:54419449-54419662 | Rare:36 | ||||
| chr12:55682163-55682251 | Common:1; Rare:24 | ||||
| chr12:55716014-55716195 | Common:1; Rare:85 | ||||
| chr12:55716403-55716554 | Common:2; Rare:42 | ||||
| chr12:55720206-55720496 | Common:4; Rare:39; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:55728301-55728508 | Rare:65 | ||||
| chr12:55728961-55729103 | Rare:25 | ||||
| chr12:55729309-55729639 | Common:2; Rare:70 | ||||
| chr12:55729671-55729807 | Rare:32 | ||||
| chr12:55829509-55829793 | Rare:92 |