| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118372846-118373165 | Common:2; Rare:83 | ||||
| chr12:119178610-119179048 | Common:1; Rare:77; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:119667794-119668008 | Common:2; Rare:60 | ||||
| chr12:120116641-120116935 | Common:5; Rare:84 | ||||
| chr12:120201081-120201319 | Common:2; Rare:78 | ||||
| chr12:120250152-120250351 | Common:1; Rare:30 | ||||
| chr12:120446326-120446483 | Common:1; Rare:70 | ||||
| chr12:120469547-120469895 | Common:3; Rare:121 | ||||
| chr12:120495845-120496249 | Common:7; Rare:134 | ||||
| chr12:120581358-120581559 | Common:1; Rare:75 | ||||
| chr12:121399910-121400180 | Common:3; Rare:104 | ||||
| chr12:121420374-121420607 | Common:2; Rare:55 | ||||
| chr12:121712659-121712844 | Common:2; Rare:70 | ||||
| chr12:121802908-121803109 | Common:1; Rare:53 | ||||
| chr12:121888649-121888868 | Common:2; Rare:69 |