| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:7089291-7089746 | Common:3; Rare:146 | ||||
| chr12:8242913-8243142 | Common:5; Rare:71 | ||||
| chr12:9070499-9070838 | Common:3; Rare:64 | ||||
| chr12:9093533-9093684 | Common:1; Rare:43; Clinvar (benign):1 | ||||
| chr12:9240324-9240394 | Common:1; Rare:14 | ||||
| chr12:9283876-9284034 | Common:4; Rare:12 | ||||
| chr12:9448179-9448310 | Common:1; Rare:68 | ||||
| chr12:9647901-9648178 | Common:4; Rare:91 | ||||
| chr12:10224928-10225069 | Rare:38 | ||||
| chr12:12808004-12808212 | Common:1; Rare:32 | ||||
| chr12:15001745-15001847 | Rare:22 | ||||
| chr12:15168108-15168317 | Common:3; Rare:27 | ||||
| chr12:15168477-15168572 | Rare:18 | ||||
| chr12:15209065-15209366 | Common:1; Rare:69 | ||||
| chr12:15218734-15219051 | Rare:63 |