| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120495875-120496168 | Common:5; Rare:96 | ||||
| chr12:121399879-121400147 | Common:5; Rare:99 | ||||
| chr12:121802919-121803091 | Rare:43 | ||||
| chr12:122526904-122527281 | Common:3; Rare:123 | ||||
| chr12:122975103-122975362 | Common:1; Rare:94 | ||||
| chr12:122980615-122980953 | Common:2; Rare:98 | ||||
| chr12:123233085-123233490 | Common:2; Rare:136; Clinvar:1 | ||||
| chr12:123584278-123584589 | Common:6; Rare:86 | ||||
| chr12:123601836-123602163 | Common:6; Rare:92 | ||||
| chr12:123633547-123633856 | Common:1; Rare:148; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123972543-123972951 | Common:6; Rare:138 | ||||
| chr12:131710822-131711097 | Rare:66 | ||||
| chr12:132144310-132144493 | Rare:75 | ||||
| chr12:132687332-132687623 | Common:2; Rare:103; Clinvar:2; Clinvar (benign):6 | ||||
| chr12:132761812-132762158 | Common:3; Rare:117 |