| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:121802940-121803086 | Rare:35 | ||||
| chr12:122266405-122266547 | Common:2; Rare:60 | ||||
| chr12:122526885-122527267 | Common:3; Rare:129 | ||||
| chr12:122752588-122752941 | Common:1; Rare:122 | ||||
| chr12:122872023-122872241 | Rare:36 | ||||
| chr12:122896058-122896231 | Rare:89 | ||||
| chr12:122980552-122980726 | Rare:56 | ||||
| chr12:123105452-123105661 | Common:1; Rare:37 | ||||
| chr12:123233109-123233512 | Common:2; Rare:134; Clinvar:1 | ||||
| chr12:123364820-123364980 | Common:3; Rare:61 | ||||
| chr12:123584334-123584609 | Common:5; Rare:91 | ||||
| chr12:123633624-123633851 | Common:1; Rare:104; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123973008-123973328 | Common:2; Rare:107 | ||||
| chr12:130871735-130872110 | Common:4; Rare:156 | ||||
| chr12:132887558-132887834 | Rare:79 |