| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122526849-122527262 | Common:4; Rare:146 | ||||
| chr12:122975170-122975252 | Common:1; Rare:27 | ||||
| chr12:122980584-122980909 | Common:1; Rare:95 | ||||
| chr12:123233093-123233490 | Common:2; Rare:132; Clinvar:1 | ||||
| chr12:123364758-123364948 | Common:3; Rare:86 | ||||
| chr12:123584325-123584660 | Common:5; Rare:119 | ||||
| chr12:123601983-123602160 | Common:3; Rare:59 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972550-123972899 | Common:6; Rare:119 | ||||
| chr12:123972989-123973312 | Common:2; Rare:103 | ||||
| chr12:124914856-124915057 | Common:3; Rare:90 | ||||
| chr12:128824002-128824108 | Common:1; Rare:35 | ||||
| chr12:130871780-130872110 | Common:4; Rare:133 | ||||
| chr12:131710805-131711119 | Rare:83 | ||||
| chr12:131949624-131949989 | Common:2; Rare:116 |