| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:12561111-12561285 | Common:1; Rare:36 | ||||
| chr12:12561620-12562034 | Common:1; Rare:102 | ||||
| chr12:12562179-12562328 | Rare:44 | ||||
| chr12:12562647-12562894 | Rare:64 | ||||
| chr12:12611559-12611678 | Common:1; Rare:30 | ||||
| chr12:12611684-12612044 | Common:2; Rare:106 | ||||
| chr12:12696096-12696313 | Common:1; Rare:53 | ||||
| chr12:12696626-12696765 | Rare:43 | ||||
| chr12:12714645-12714808 | Common:1; Rare:43 | ||||
| chr12:12716552-12716770 | Common:3; Rare:50 | ||||
| chr12:12716956-12717638 | Common:3; Rare:220; Clinvar:3; Clinvar (benign):3 | ||||
| chr12:12725020-12725491 | Common:4; Rare:121 | ||||
| chr12:12725504-12726057 | Common:6; Rare:134 | ||||
| chr12:12785080-12785214 | Rare:22 | ||||
| chr12:12785231-12785692 | Common:2; Rare:92 |