| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:120437827-120438324 | Common:13; Rare:587; Clinvar (benign):8; Clinvar (pathogenic):1 | ||||
| chr12:120445717-120446523 | Common:12; Rare:667 | ||||
| chr12:120446507-120446968 | Common:7; Rare:397; Clinvar (pathogenic):3 | ||||
| chr12:120469136-120469536 | Common:9; Rare:296 | ||||
| chr12:120469478-120470280 | Common:26; Rare:914 | ||||
| chr12:120470307-120470715 | Common:6; Rare:165 | ||||
| chr12:120495481-120496264 | Common:51; Rare:857 | ||||
| chr12:120528677-120529397 | Common:9; Rare:479 | ||||
| chr12:120534104-120534510 | Common:5; Rare:237 | ||||
| chr12:120534702-120535263 | Common:3; Rare:330 | ||||
| chr12:120581277-120581677 | Common:9; Rare:578 | ||||
| chr12:120581759-120582159 | Common:4; Rare:66 | ||||
| chr12:120640368-120640856 | Common:1; Rare:374 | ||||
| chr12:120686286-120686759 | Common:10; Rare:347 | ||||
| chr12:120686730-120687223 | Common:8; Rare:543 |