| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:119667745-119668003 | Common:2; Rare:71 | ||||
| chr12:119877261-119877518 | Common:2; Rare:60 | ||||
| chr12:120116705-120116944 | Common:3; Rare:79 | ||||
| chr12:120194683-120194784 | Rare:36 | ||||
| chr12:120201070-120201360 | Common:2; Rare:93 | ||||
| chr12:120437914-120437959 | Rare:9 | ||||
| chr12:120438018-120438228 | Rare:93; Clinvar (benign):2 | ||||
| chr12:120446321-120446495 | Common:2; Rare:77 | ||||
| chr12:120469524-120469912 | Common:4; Rare:133 | ||||
| chr12:120495845-120496550 | Common:7; Rare:232 | ||||
| chr12:120581341-120581559 | Common:1; Rare:79 | ||||
| chr12:120686967-120687163 | Common:1; Rare:68 | ||||
| chr12:121399838-121400160 | Common:5; Rare:122 | ||||
| chr12:121580226-121580368 | Rare:47 | ||||
| chr12:121802919-121803138 | Common:1; Rare:55 |