| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123232819-123232919 | Common:1; Rare:27 | ||||
| chr12:123233081-123233506 | Common:3; Rare:145; Clinvar:1 | ||||
| chr12:123364820-123364977 | Common:3; Rare:61 | ||||
| chr12:123383950-123384149 | Rare:44 | ||||
| chr12:123584430-123584657 | Common:2; Rare:99 | ||||
| chr12:123601829-123602164 | Common:6; Rare:94 | ||||
| chr12:123633624-123633887 | Common:2; Rare:123; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123671016-123671129 | Common:1; Rare:25 | ||||
| chr12:130871723-130872122 | Common:4; Rare:167 | ||||
| chr12:131710770-131711125 | Rare:101 | ||||
| chr12:131929033-131929306 | Common:10; Rare:83; Clinvar:1 | ||||
| chr12:132084069-132084296 | Common:5; Rare:77 | ||||
| chr12:132632874-132633002 | Rare:25 | ||||
| chr12:132687409-132687729 | Common:4; Rare:105 | ||||
| chr12:132710557-132711035 | Common:5; Rare:154 |