| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:389539-389662 | Common:5; Rare:56 | ||||
| chr12:401434-401664 | Common:1; Rare:63 | ||||
| chr12:643616-643709 | Rare:18 | ||||
| chr12:991095-991342 | Common:4; Rare:108 | ||||
| chr12:2004427-2004639 | Common:1; Rare:72 | ||||
| chr12:2795036-2795236 | Rare:78 | ||||
| chr12:2812489-2812727 | Common:1; Rare:59 | ||||
| chr12:2812880-2813017 | Rare:42 | ||||
| chr12:2877031-2877277 | Rare:82 | ||||
| chr12:2890685-2890938 | Common:1; Rare:103 | ||||
| chr12:3077257-3077439 | Common:7; Rare:79 | ||||
| chr12:3873307-3873514 | Common:4; Rare:44 | ||||
| chr12:4320957-4321258 | Common:5; Rare:113 | ||||
| chr12:4538436-4538907 | Common:1; Rare:104 | ||||
| chr12:4649010-4649149 | Common:2; Rare:48; Clinvar (benign):1 |