| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103965705-103966040 | Common:4; Rare:80 | ||||
| chr12:104064435-104064614 | Rare:47 | ||||
| chr12:104138142-104138403 | Common:1; Rare:67 | ||||
| chr12:104286878-104287121 | Common:3; Rare:55 | ||||
| chr12:104287204-104287322 | Rare:27 | ||||
| chr12:104986220-104986346 | Common:2; Rare:39 | ||||
| chr12:105107612-105107824 | Common:1; Rare:98; Clinvar:1 | ||||
| chr12:105176126-105176170 | Rare:10 | ||||
| chr12:105177231-105177343 | Rare:43 | ||||
| chr12:105188725-105188866 | Rare:28 | ||||
| chr12:105195445-105195733 | Common:1; Rare:87 | ||||
| chr12:105235439-105235526 | Common:2; Rare:14 | ||||
| chr12:105236001-105236279 | Common:3; Rare:112 | ||||
| chr12:106357690-106357812 | Common:3; Rare:28; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:106955648-106955930 | Rare:100 |