| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:47812630-47812698 | Rare:12 | ||||
| chr12:47813012-47813075 | Rare:16 | ||||
| chr12:47819854-47820237 | Common:5; Rare:92 | ||||
| chr12:47820423-47820910 | Rare:67 | ||||
| chr12:47904964-47905164 | Common:1; Rare:62; Clinvar:1 | ||||
| chr12:47963379-47963662 | Common:3; Rare:69 | ||||
| chr12:48105482-48105670 | Common:1; Rare:33 | ||||
| chr12:48105843-48106469 | Common:2; Rare:178 | ||||
| chr12:48119127-48119429 | Common:2; Rare:61; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48119693-48119743 | Rare:7 | ||||
| chr12:48119936-48119999 | Rare:9 | ||||
| chr12:48157436-48157740 | Common:4; Rare:74 | ||||
| chr12:48350769-48351135 | Common:6; Rare:129 | ||||
| chr12:48351194-48351408 | Common:2; Rare:39 | ||||
| chr12:48681430-48681582 | Rare:37 |