| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:71839612-71839821 | Common:1; Rare:84 | ||||
| chr12:72272275-72272444 | Common:2; Rare:40 | ||||
| chr12:74537701-74537889 | Common:1; Rare:73 | ||||
| chr12:75390870-75391336 | Common:2; Rare:165 | ||||
| chr12:75511521-75511907 | Rare:113 | ||||
| chr12:76053089-76053360 | Common:1; Rare:72 | ||||
| chr12:76083907-76084189 | Common:1; Rare:79 | ||||
| chr12:76084566-76084857 | Common:1; Rare:95 | ||||
| chr12:76085044-76085113 | Common:2; Rare:21 | ||||
| chr12:76348347-76348540 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):1 | ||||
| chr12:76559571-76559924 | Common:2; Rare:122 | ||||
| chr12:76763985-76764302 | Common:3; Rare:133 | ||||
| chr12:76878812-76879224 | Common:1; Rare:129 | ||||
| chr12:77065473-77065830 | Common:2; Rare:115 | ||||
| chr12:78863513-78863702 | Common:3; Rare:45 |