| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:114683712-114684051 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:114684497-114684687 | Rare:57 | ||||
| chr12:118016551-118016795 | Common:2; Rare:51 | ||||
| chr12:118135938-118136200 | Common:2; Rare:82 | ||||
| chr12:118372846-118373165 | Common:2; Rare:83 | ||||
| chr12:119178545-119178847 | Common:1; Rare:61; Clinvar:1 | ||||
| chr12:120116655-120116946 | Common:5; Rare:89 | ||||
| chr12:120194693-120194798 | Rare:39 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120437853-120438222 | Common:2; Rare:137; Clinvar (benign):2 | ||||
| chr12:120446331-120446483 | Common:1; Rare:68 | ||||
| chr12:120469482-120469895 | Common:5; Rare:139 | ||||
| chr12:120495859-120496550 | Common:7; Rare:229 | ||||
| chr12:120581353-120581577 | Common:1; Rare:78 | ||||
| chr12:121210037-121210146 | Common:2; Rare:33 |