| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:45215976-45216300 | Common:1; Rare:98 | ||||
| chr12:46267310-46267472 | Rare:33 | ||||
| chr12:46268479-46269146 | Common:3; Rare:168 | ||||
| chr12:46269158-46269192 | Rare:7 | ||||
| chr12:46371230-46371514 | Common:2; Rare:122 | ||||
| chr12:46372641-46372963 | Rare:134 | ||||
| chr12:47705955-47706082 | Rare:56 | ||||
| chr12:47758878-47759027 | Common:1; Rare:33 | ||||
| chr12:47963355-47963668 | Common:3; Rare:77 | ||||
| chr12:48004472-48004645 | Common:2; Rare:32; Clinvar (benign):1 | ||||
| chr12:48105713-48105948 | Common:2; Rare:51 | ||||
| chr12:48105962-48106105 | Rare:38 | ||||
| chr12:48119181-48119397 | Common:2; Rare:42; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48350832-48351065 | Common:5; Rare:89 | ||||
| chr12:48682204-48682467 | Common:4; Rare:76 |