| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112013125-112013467 | Common:1; Rare:121 | ||||
| chr12:112108735-112108822 | Rare:29 | ||||
| chr12:112125341-112125587 | Rare:65 | ||||
| chr12:113185435-113185777 | Common:8; Rare:124 | ||||
| chr12:113221020-113221319 | Common:2; Rare:85 | ||||
| chr12:113244283-113244390 | Rare:16 | ||||
| chr12:113966299-113966466 | Common:3; Rare:51 | ||||
| chr12:114404193-114404349 | Rare:44 | ||||
| chr12:114405781-114405883 | Common:1; Rare:17 | ||||
| chr12:114405984-114406277 | Common:1; Rare:61 | ||||
| chr12:114407931-114408208 | Common:1; Rare:47; Clinvar (benign):2 | ||||
| chr12:114408555-114408993 | Rare:89 | ||||
| chr12:114683964-114684292 | Common:3; Rare:93; Clinvar:2 | ||||
| chr12:117099315-117099532 | Common:1; Rare:71 | ||||
| chr12:118061044-118061407 | Common:3; Rare:85 |