| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:119667480-119668060 | Common:2; Rare:134 | ||||
| chr12:119877230-119877623 | Common:3; Rare:86 | ||||
| chr12:120116723-120117019 | Common:6; Rare:115 | ||||
| chr12:120117080-120117360 | Common:3; Rare:82 | ||||
| chr12:120194645-120194818 | Common:1; Rare:72 | ||||
| chr12:120201069-120201422 | Common:2; Rare:112 | ||||
| chr12:120265688-120265802 | Rare:66 | ||||
| chr12:120361350-120361710 | Common:2; Rare:65 | ||||
| chr12:120361730-120362050 | Rare:69 | ||||
| chr12:120367470-120367676 | Rare:32 | ||||
| chr12:120367844-120368244 | Rare:129 | ||||
| chr12:120368247-120368468 | Common:2; Rare:55 | ||||
| chr12:120369162-120369339 | Rare:45 | ||||
| chr12:120437972-120438135 | Common:1; Rare:54; Clinvar (benign):1 | ||||
| chr12:120446322-120446509 | Common:2; Rare:83 |