| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:103930068-103930529 | Common:8; Rare:155 | ||||
| chr12:103957138-103957335 | Common:5; Rare:59 | ||||
| chr12:103965704-103966027 | Common:4; Rare:75 | ||||
| chr12:104138170-104138406 | Common:1; Rare:65 | ||||
| chr12:105107612-105107789 | Common:1; Rare:80 | ||||
| chr12:106955657-106955846 | Rare:61 | ||||
| chr12:107685689-107685845 | Rare:51 | ||||
| chr12:108561141-108561448 | Common:3; Rare:74 | ||||
| chr12:108562394-108562645 | Common:5; Rare:99; Clinvar:2; Clinvar (benign):1 | ||||
| chr12:109097920-109098216 | Common:5; Rare:91 | ||||
| chr12:109477293-109477643 | Common:3; Rare:82 | ||||
| chr12:109573478-109573813 | Common:3; Rare:99; Clinvar:4; Clinvar (benign):5 | ||||
| chr12:109900159-109900348 | Rare:66 | ||||
| chr12:109996223-109996445 | Common:2; Rare:67 | ||||
| chr12:109998918-109999213 | Rare:47 |