| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134223911-134224166 | Common:2; Rare:87 | ||||
| chr11:134224533-134224690 | Rare:58 | ||||
| chr11:134253280-134253608 | Common:2; Rare:118; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr12:388169-388390 | Common:2; Rare:62 | ||||
| chr12:389230-389425 | Common:1; Rare:79 | ||||
| chr12:389442-389662 | Common:5; Rare:86 | ||||
| chr12:401420-401664 | Common:2; Rare:70 | ||||
| chr12:643624-643928 | Common:2; Rare:63 | ||||
| chr12:752323-752602 | Common:1; Rare:79 | ||||
| chr12:990491-990580 | Common:1; Rare:26 | ||||
| chr12:990765-990873 | Rare:31 | ||||
| chr12:991080-991342 | Common:5; Rare:113 | ||||
| chr12:1690873-1691099 | Common:2; Rare:81 | ||||
| chr12:1811736-1811884 | Common:1; Rare:34 | ||||
| chr12:2004230-2004245 | Rare:7 |