| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:107093514-107093612 | Rare:40 | ||||
| chr12:107685717-107685895 | Rare:63 | ||||
| chr12:108562394-108562651 | Common:6; Rare:103; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:109052474-109052644 | Common:3; Rare:47 | ||||
| chr12:109093618-109093903 | Common:2; Rare:64 | ||||
| chr12:109154535-109154684 | Common:1; Rare:39 | ||||
| chr12:109477292-109477638 | Common:3; Rare:81 | ||||
| chr12:109573472-109573813 | Common:3; Rare:102; Clinvar:4; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
| chr12:109880379-109880721 | Common:2; Rare:99 | ||||
| chr12:110281024-110281164 | Rare:58 | ||||
| chr12:110468670-110468909 | Rare:59 | ||||
| chr12:110502037-110502331 | Common:1; Rare:105 | ||||
| chr12:110613997-110614187 | Rare:55; Clinvar:2; Clinvar (benign):2 | ||||
| chr12:111685978-111686103 | Rare:43 | ||||
| chr12:111841896-111842230 | Common:3; Rare:89 |