| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:42237598-42237958 | Common:4; Rare:148 | ||||
| chr12:42238165-42238522 | Common:6; Rare:291 | ||||
| chr12:42326025-42326246 | Common:5; Rare:205 | ||||
| chr12:42589576-42590546 | Common:7; Rare:394; Clinvar:10; Clinvar (benign):2 | ||||
| chr12:43758571-43759127 | Common:14; Rare:318; Clinvar:6 | ||||
| chr12:43759285-43759685 | Common:2; Rare:116 | ||||
| chr12:43806030-43806210 | Common:4; Rare:165 | ||||
| chr12:43806216-43806511 | Common:7; Rare:174 | ||||
| chr12:43835380-43836190 | Common:5; Rare:311 | ||||
| chr12:43836200-43836850 | Common:10; Rare:283 | ||||
| chr12:44876162-44876513 | Common:4; Rare:161 | ||||
| chr12:44876701-44876897 | Common:2; Rare:53 | ||||
| chr12:45215405-45215726 | Common:1; Rare:98 | ||||
| chr12:45215853-45216217 | Common:7; Rare:264 | ||||
| chr12:45729254-45730669 | Common:9; Rare:952; Clinvar:4 |