| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:123972564-123972895 | Common:6; Rare:114 | ||||
| chr12:124786462-124786789 | Common:3; Rare:89 | ||||
| chr12:130839139-130839393 | Common:2; Rare:92 | ||||
| chr12:130871694-130872122 | Common:4; Rare:177 | ||||
| chr12:131710779-131711119 | Rare:95 | ||||
| chr12:132687303-132687713 | Common:4; Rare:151; Clinvar:7; Clinvar (benign):10; Clinvar (pathogenic):1 | ||||
| chr12:132829048-132829216 | Rare:81 | ||||
| chr12:132887558-132887798 | Rare:71 | ||||
| chr12:132956252-132956426 | Common:1; Rare:38 | ||||
| chr12:132986236-132986428 | Rare:40 | ||||
| chr12:133130242-133130573 | Common:6; Rare:102 | ||||
| chr13:19633416-19633773 | Common:1; Rare:132 | ||||
| chr13:19782927-19783088 | Common:2; Rare:57 | ||||
| chr13:19863441-19863657 | Common:3; Rare:70 | ||||
| chr13:20566818-20567205 | Common:1; Rare:113 |