| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:118061044-118061407 | Common:3; Rare:85 | ||||
| chr12:118135917-118136224 | Common:2; Rare:94 | ||||
| chr12:118372866-118373165 | Common:1; Rare:76 | ||||
| chr12:119178614-119178933 | Common:1; Rare:56; Clinvar:1; Clinvar (benign):1 | ||||
| chr12:120064180-120064631 | Common:1; Rare:77 | ||||
| chr12:120116720-120116935 | Common:2; Rare:71 | ||||
| chr12:120201081-120201366 | Common:2; Rare:90 | ||||
| chr12:120446353-120446474 | Common:1; Rare:55 | ||||
| chr12:120469554-120469912 | Common:3; Rare:125 | ||||
| chr12:120495845-120496246 | Common:7; Rare:134 | ||||
| chr12:120529127-120529198 | Common:1; Rare:24 | ||||
| chr12:120686967-120687155 | Common:1; Rare:65 | ||||
| chr12:121210035-121210161 | Common:2; Rare:44 | ||||
| chr12:121296669-121296931 | Common:1; Rare:82 | ||||
| chr12:121580226-121580519 | Rare:81 |