| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:122980163-122980256 | Rare:31 | ||||
| chr12:122980389-122980726 | Rare:113 | ||||
| chr12:123233087-123233512 | Common:2; Rare:145; Clinvar:1 | ||||
| chr12:123268210-123268329 | Rare:19 | ||||
| chr12:123364825-123364983 | Common:3; Rare:58 | ||||
| chr12:123436466-123436579 | Rare:21 | ||||
| chr12:123457863-123458196 | Common:1; Rare:66 | ||||
| chr12:123584351-123584609 | Common:5; Rare:90 | ||||
| chr12:123601819-123602174 | Common:6; Rare:99 | ||||
| chr12:123633611-123633872 | Common:2; Rare:127; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972530-123972656 | Common:3; Rare:36 | ||||
| chr12:124786469-124786796 | Common:3; Rare:87 | ||||
| chr12:124917676-124917784 | Rare:31 | ||||
| chr12:128853309-128853629 | Common:4; Rare:83 | ||||
| chr12:130716247-130716335 | Rare:16 |