| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:112938295-112938433 | Common:1; Rare:25 | ||||
| chr12:113185435-113185777 | Common:8; Rare:124 | ||||
| chr12:113221019-113221319 | Common:2; Rare:86 | ||||
| chr12:113335060-113335235 | Rare:61 | ||||
| chr12:113966223-113966437 | Common:4; Rare:67 | ||||
| chr12:114684146-114684353 | Rare:54 | ||||
| chr12:116738064-116738343 | Common:3; Rare:80 | ||||
| chr12:117190419-117190587 | Rare:74 | ||||
| chr12:118016565-118016801 | Common:1; Rare:47 | ||||
| chr12:118135946-118136232 | Common:2; Rare:90 | ||||
| chr12:118372866-118373165 | Common:1; Rare:76 | ||||
| chr12:119178706-119178950 | Common:1; Rare:39; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:119668078-119668150 | Common:1; Rare:15 | ||||
| chr12:120116651-120116938 | Common:5; Rare:85 | ||||
| chr12:120194690-120194791 | Rare:37 |