| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:134253290-134253592 | Common:2; Rare:104; Clinvar (benign):1 | ||||
| chr12:389242-389371 | Rare:47 | ||||
| chr12:389481-389680 | Common:5; Rare:87 | ||||
| chr12:401408-401678 | Common:2; Rare:76 | ||||
| chr12:752338-752597 | Common:1; Rare:75 | ||||
| chr12:989692-989998 | Rare:70 | ||||
| chr12:990735-990844 | Rare:31 | ||||
| chr12:991085-991322 | Common:4; Rare:106 | ||||
| chr12:1690866-1691082 | Common:2; Rare:79 | ||||
| chr12:2004420-2004685 | Common:2; Rare:86 | ||||
| chr12:2812608-2812773 | Common:1; Rare:61 | ||||
| chr12:2812878-2813013 | Rare:41 | ||||
| chr12:2876918-2877276 | Common:1; Rare:111 | ||||
| chr12:2890690-2890935 | Common:1; Rare:97 | ||||
| chr12:2958896-2959042 | Common:2; Rare:41 |