| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118061046-118061286 | Common:1; Rare:70 | ||||
| chr12:118135946-118136305 | Common:2; Rare:111 | ||||
| chr12:118372650-118372706 | Rare:12 | ||||
| chr12:118372758-118373189 | Common:2; Rare:114 | ||||
| chr12:118376677-118376810 | Rare:39 | ||||
| chr12:119178615-119178944 | Common:1; Rare:59; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119668076-119668203 | Common:1; Rare:28 | ||||
| chr12:120116684-120116878 | Common:1; Rare:56 | ||||
| chr12:120168711-120168983 | Common:2; Rare:68 | ||||
| chr12:120196933-120196954 | Rare:5 | ||||
| chr12:120197463-120197922 | Common:4; Rare:115 | ||||
| chr12:120200834-120201366 | Common:3; Rare:164 | ||||
| chr12:120215382-120215665 | Rare:108 | ||||
| chr12:120216078-120216169 | Rare:14 | ||||
| chr12:120224567-120224847 | Common:3; Rare:79 |