| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:62260040-62260493 | Common:1; Rare:166 | ||||
| chr12:62466714-62466870 | Rare:47 | ||||
| chr12:63779779-63780175 | Common:3; Rare:162; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):3 | ||||
| chr12:64222233-64222349 | Rare:43 | ||||
| chr12:64452039-64452174 | Common:1; Rare:49 | ||||
| chr12:64610285-64610621 | Common:4; Rare:122 | ||||
| chr12:64759373-64759494 | Common:1; Rare:40; Clinvar:3 | ||||
| chr12:65824970-65825122 | Rare:38 | ||||
| chr12:66130694-66130861 | Rare:60 | ||||
| chr12:67269557-67269706 | Common:1; Rare:61 | ||||
| chr12:67648600-67648804 | Common:1; Rare:60 | ||||
| chr12:68332265-68332636 | Common:1; Rare:124 | ||||
| chr12:68610724-68611050 | Common:1; Rare:130 | ||||
| chr12:68686837-68687056 | Common:3; Rare:68 | ||||
| chr12:68807791-68808270 | Common:5; Rare:129 |