| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123268189-123268314 | Rare:25 | ||||
| chr12:123364820-123364977 | Common:3; Rare:61 | ||||
| chr12:123584334-123584604 | Common:5; Rare:87 | ||||
| chr12:123601832-123602198 | Common:6; Rare:107 | ||||
| chr12:123633617-123633851 | Common:1; Rare:110; Clinvar:8; Clinvar (benign):1 | ||||
| chr12:123670995-123671143 | Common:1; Rare:33 | ||||
| chr12:123931318-123931358 | Rare:20 | ||||
| chr12:124914633-124914993 | Common:3; Rare:133 | ||||
| chr12:128823804-128824113 | Common:2; Rare:107 | ||||
| chr12:130716258-130716336 | Rare:13 | ||||
| chr12:130839129-130839386 | Common:2; Rare:91 | ||||
| chr12:130871755-130872116 | Common:4; Rare:145 | ||||
| chr12:131710839-131711130 | Common:1; Rare:73 | ||||
| chr12:131929014-131929271 | Common:10; Rare:78; Clinvar:1 | ||||
| chr12:132084146-132084303 | Common:4; Rare:57 |