| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:389229-389347 | Rare:47 | ||||
| chr12:401446-401664 | Rare:58 | ||||
| chr12:610367-610454 | Rare:9 | ||||
| chr12:643609-643757 | Rare:30 | ||||
| chr12:752306-752597 | Common:1; Rare:86 | ||||
| chr12:990425-990605 | Common:1; Rare:47 | ||||
| chr12:991093-991318 | Common:3; Rare:104 | ||||
| chr12:2812516-2812727 | Common:1; Rare:54 | ||||
| chr12:2877038-2877262 | Rare:68 | ||||
| chr12:3077249-3077434 | Common:6; Rare:81 | ||||
| chr12:3873355-3873581 | Common:2; Rare:53 | ||||
| chr12:4320943-4321260 | Common:5; Rare:121 | ||||
| chr12:4538436-4538914 | Common:2; Rare:104 | ||||
| chr12:4649026-4649171 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chr12:5431950-5432128 | Common:4; Rare:71 |