| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:389521-389650 | Common:5; Rare:59 | ||||
| chr12:401446-401637 | Rare:48 | ||||
| chr12:643620-643920 | Common:2; Rare:63 | ||||
| chr12:2812609-2812713 | Common:1; Rare:34 | ||||
| chr12:2877031-2877254 | Rare:68 | ||||
| chr12:2890706-2890941 | Common:1; Rare:94 | ||||
| chr12:3077261-3077428 | Common:5; Rare:71 | ||||
| chr12:4320957-4321258 | Common:5; Rare:113 | ||||
| chr12:4538457-4538914 | Common:2; Rare:96 | ||||
| chr12:4649045-4649178 | Common:1; Rare:52; Clinvar (benign):2 | ||||
| chr12:6124528-6124762 | Rare:32; Clinvar:1 | ||||
| chr12:6200042-6200557 | Common:4; Rare:151 | ||||
| chr12:6375346-6375624 | Common:3; Rare:70; Clinvar:1; Clinvar (benign):5 | ||||
| chr12:6470648-6470757 | Rare:37 | ||||
| chr12:6493212-6493386 | Common:6; Rare:49 |