| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118359096-118359195 | Rare:13 | ||||
| chr12:118372887-118373220 | Common:1; Rare:86 | ||||
| chr12:119877279-119877518 | Common:2; Rare:52 | ||||
| chr12:120194690-120194784 | Rare:33 | ||||
| chr12:120201082-120201354 | Common:2; Rare:88 | ||||
| chr12:120437850-120438147 | Common:2; Rare:99; Clinvar (benign):1 | ||||
| chr12:120446353-120446475 | Common:1; Rare:56 | ||||
| chr12:120469618-120469867 | Common:2; Rare:89 | ||||
| chr12:120495900-120496143 | Common:3; Rare:72 | ||||
| chr12:120529137-120529233 | Common:1; Rare:27 | ||||
| chr12:121580240-121580384 | Rare:53 | ||||
| chr12:121888642-121888863 | Common:2; Rare:73 | ||||
| chr12:121918402-121918618 | Common:5; Rare:47 | ||||
| chr12:122021677-122022083 | Common:9; Rare:112 | ||||
| chr12:122266405-122266619 | Common:2; Rare:76 |