| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:69239424-69239652 | Common:2; Rare:95 | ||||
| chr12:69359627-69359781 | Common:4; Rare:67 | ||||
| chr12:69359963-69359997 | Rare:10 | ||||
| chr12:69470234-69470476 | Common:4; Rare:101 | ||||
| chr12:69585276-69585516 | Common:4; Rare:98 | ||||
| chr12:69738575-69738940 | Common:4; Rare:133 | ||||
| chr12:71663822-71664030 | Common:1; Rare:56 | ||||
| chr12:71664117-71664309 | Rare:45 | ||||
| chr12:71839646-71839807 | Common:1; Rare:63 | ||||
| chr12:74537717-74537873 | Common:1; Rare:60 | ||||
| chr12:75390891-75391105 | Common:1; Rare:66 | ||||
| chr12:76083898-76084076 | Rare:53 | ||||
| chr12:76348357-76348561 | Common:2; Rare:73; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:76763978-76764261 | Common:3; Rare:116 | ||||
| chr12:76878946-76879182 | Rare:83 |