| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064451-104064560 | Rare:28 | ||||
| chr12:104138147-104138375 | Rare:56 | ||||
| chr12:104286770-104287065 | Common:3; Rare:55 | ||||
| chr12:104287204-104287268 | Rare:10 | ||||
| chr12:104958254-104958446 | Common:3; Rare:55 | ||||
| chr12:105107594-105107797 | Common:1; Rare:95 | ||||
| chr12:105236036-105236352 | Common:3; Rare:141 | ||||
| chr12:106357988-106358100 | Common:3; Rare:45 | ||||
| chr12:106955648-106955917 | Rare:96 | ||||
| chr12:106956652-106956922 | Rare:49 | ||||
| chr12:106987071-106987283 | Common:4; Rare:57 | ||||
| chr12:107685638-107685917 | Common:2; Rare:89 | ||||
| chr12:108339253-108339532 | Common:2; Rare:71 | ||||
| chr12:108561136-108561422 | Common:2; Rare:71 | ||||
| chr12:108562371-108562658 | Common:8; Rare:115; Clinvar:2; Clinvar (benign):3 |