| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120495835-120496228 | Common:8; Rare:130 | ||||
| chr12:120529063-120529285 | Common:2; Rare:81 | ||||
| chr12:120534092-120534410 | Common:2; Rare:83 | ||||
| chr12:120534953-120535033 | Rare:32 | ||||
| chr12:120535044-120535048 | |||||
| chr12:120581291-120581678 | Common:2; Rare:137 | ||||
| chr12:120686262-120686624 | Common:3; Rare:97 | ||||
| chr12:120686925-120687210 | Common:2; Rare:100 | ||||
| chr12:120710339-120710543 | Common:3; Rare:76 | ||||
| chr12:120710660-120710725 | Rare:10 | ||||
| chr12:120725700-120725915 | Common:2; Rare:68; Clinvar:1; Clinvar (pathogenic):1 | ||||
| chr12:120903433-120903686 | Rare:55 | ||||
| chr12:120904201-120904547 | Common:4; Rare:131 | ||||
| chr12:121015944-121016204 | Common:1; Rare:52 | ||||
| chr12:121038905-121039286 | Common:3; Rare:82 |