| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:6598040-6598360 | Common:1; Rare:84 | ||||
| chr12:6606589-6606724 | Rare:44 | ||||
| chr12:6663102-6663403 | Common:2; Rare:83 | ||||
| chr12:6688843-6689081 | Rare:74 | ||||
| chr12:6689386-6689748 | Common:3; Rare:97 | ||||
| chr12:6723966-6724296 | Rare:80 | ||||
| chr12:6752945-6753189 | Common:6; Rare:77 | ||||
| chr12:6851922-6852220 | Rare:75 | ||||
| chr12:6867384-6867604 | Common:2; Rare:114; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:6873291-6873541 | Common:1; Rare:73 | ||||
| chr12:6904723-6904847 | Rare:35 | ||||
| chr12:6943531-6943817 | Common:4; Rare:116 | ||||
| chr12:6970640-6970979 | Common:4; Rare:111; Clinvar (benign):1 | ||||
| chr12:7018430-7018563 | Common:1; Rare:46 | ||||
| chr12:7108460-7108681 | Common:1; Rare:65 |