| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123233087-123233504 | Common:2; Rare:142; Clinvar:1 | ||||
| chr12:123364814-123364977 | Common:3; Rare:63 | ||||
| chr12:123584283-123584669 | Common:8; Rare:135 | ||||
| chr12:123601794-123602174 | Common:6; Rare:106 | ||||
| chr12:123633579-123633868 | Common:2; Rare:143; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972555-123972934 | Common:6; Rare:127 | ||||
| chr12:124388797-124388978 | Common:3; Rare:53 | ||||
| chr12:124786464-124786789 | Common:3; Rare:88 | ||||
| chr12:128824070-128824108 | Common:1; Rare:16 | ||||
| chr12:131710825-131711107 | Rare:67 | ||||
| chr12:131929236-131929296 | Rare:23; Clinvar:1 | ||||
| chr12:132286445-132286670 | Common:2; Rare:61 | ||||
| chr12:132687288-132687689 | Common:4; Rare:149; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132829075-132829228 | Rare:76 | ||||
| chr12:132887553-132887861 | Rare:92 |