| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:52281126-52281272 | Common:3; Rare:28 | ||||
| chr12:52287543-52287863 | Common:8; Rare:174 | ||||
| chr12:52288029-52288349 | Common:4; Rare:155; Clinvar (pathogenic):1 | ||||
| chr12:52304834-52305025 | Common:2; Rare:62 | ||||
| chr12:52306710-52307010 | Rare:95 | ||||
| chr12:52308150-52308450 | Common:1; Rare:106 | ||||
| chr12:52319170-52319680 | Common:12; Rare:310; Clinvar:7; Clinvar (benign):10 | ||||
| chr12:52345753-52346428 | Common:4; Rare:180 | ||||
| chr12:52347090-52347680 | Common:10; Rare:118 | ||||
| chr12:52655795-52655906 | Common:1; Rare:17 | ||||
| chr12:52860075-52860428 | Common:1; Rare:127 | ||||
| chr12:52867609-52868009 | Common:3; Rare:158 | ||||
| chr12:52871258-52872119 | Common:8; Rare:256 | ||||
| chr12:52873500-52874090 | Common:13; Rare:113 | ||||
| chr12:52874120-52874550 | Common:41; Rare:305 |