| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123633620-123633856 | Common:1; Rare:111; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:130839151-130839386 | Common:2; Rare:86 | ||||
| chr12:130871697-130872122 | Common:4; Rare:176 | ||||
| chr12:131710776-131711107 | Rare:92 | ||||
| chr12:131928984-131929271 | Common:10; Rare:85; Clinvar:1 | ||||
| chr12:132687288-132687651 | Common:2; Rare:135; Clinvar:11; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132887555-132887820 | Rare:78 | ||||
| chr12:132956276-132956410 | Common:1; Rare:29 | ||||
| chr12:132986242-132986421 | Rare:39 | ||||
| chr12:133130226-133130592 | Common:7; Rare:114 | ||||
| chr13:19633391-19633746 | Common:1; Rare:133 | ||||
| chr13:21140377-21140614 | Rare:109 | ||||
| chr13:21176473-21176713 | Common:2; Rare:107 | ||||
| chr13:23889298-23889595 | Common:1; Rare:103 | ||||
| chr13:24512739-24512850 | Common:3; Rare:33 |