| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:13099404-13099509 | Rare:13 | ||||
| chr12:21508291-21508398 | Common:1; Rare:20 | ||||
| chr12:25386103-25386378 | Common:1; Rare:114 | ||||
| chr12:49230877-49231135 | Rare:48 | ||||
| chr12:49233674-49234175 | Common:3; Rare:86 | ||||
| chr12:51242257-51242429 | Rare:54 | ||||
| chr12:51320835-51320981 | Common:5; Rare:34 | ||||
| chr12:52007644-52007746 | Common:1; Rare:19 | ||||
| chr12:53381950-53382221 | Common:2; Rare:72 | ||||
| chr12:54368874-54369259 | Common:1; Rare:64 | ||||
| chr12:54423272-54423488 | Rare:39 | ||||
| chr12:56111226-56111530 | Rare:77 | ||||
| chr12:56133650-56133796 | Rare:37 | ||||
| chr12:56225496-56225672 | Rare:52 | ||||
| chr12:56355689-56355981 | Common:2; Rare:60; Clinvar:1; Clinvar (benign):1 |