| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526849-122527291 | Common:4; Rare:162 | ||||
| chr12:122975203-122975254 | Rare:19 | ||||
| chr12:122980570-122980743 | Common:1; Rare:57 | ||||
| chr12:123233081-123233496 | Common:3; Rare:142; Clinvar:1 | ||||
| chr12:123364825-123364972 | Common:2; Rare:58 | ||||
| chr12:123436161-123436318 | Rare:49 | ||||
| chr12:123584278-123584609 | Common:6; Rare:107 | ||||
| chr12:123602018-123602146 | Common:3; Rare:40 | ||||
| chr12:123633608-123633856 | Common:1; Rare:119; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972545-123972899 | Common:6; Rare:120 | ||||
| chr12:124518522-124518744 | Rare:57 | ||||
| chr12:130871694-130872122 | Common:4; Rare:177 | ||||
| chr12:130953740-130953998 | Rare:50 | ||||
| chr12:131710825-131711119 | Rare:72 | ||||
| chr12:131949624-131950021 | Common:2; Rare:133 |