| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:104064435-104064606 | Rare:42 | ||||
| chr12:104138145-104138371 | Rare:53 | ||||
| chr12:104286750-104287164 | Common:3; Rare:75 | ||||
| chr12:104287204-104287430 | Rare:59 | ||||
| chr12:105107619-105107803 | Common:1; Rare:89; Clinvar:1 | ||||
| chr12:105236084-105236341 | Common:2; Rare:121 | ||||
| chr12:106357988-106358111 | Common:3; Rare:48 | ||||
| chr12:106956657-106956922 | Rare:48 | ||||
| chr12:107093514-107093642 | Rare:49 | ||||
| chr12:107685709-107685895 | Rare:66 | ||||
| chr12:108561141-108561461 | Common:4; Rare:78 | ||||
| chr12:109477275-109477662 | Common:3; Rare:99 | ||||
| chr12:109573435-109573840 | Common:3; Rare:131; Clinvar:6; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109880357-109880676 | Common:1; Rare:96 | ||||
| chr12:109996273-109996434 | Common:2; Rare:47 |