| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:48119200-48119398 | Common:2; Rare:39; Clinvar:4; Clinvar (benign):2 | ||||
| chr12:48183492-48183677 | Common:1; Rare:45 | ||||
| chr12:48183758-48184149 | Common:5; Rare:93 | ||||
| chr12:48350787-48350957 | Rare:64 | ||||
| chr12:48682187-48682446 | Common:5; Rare:84 | ||||
| chr12:48716668-48717046 | Common:4; Rare:115 | ||||
| chr12:48814741-48814943 | Rare:33 | ||||
| chr12:48815369-48815664 | Common:1; Rare:68 | ||||
| chr12:48818339-48818526 | Rare:66 | ||||
| chr12:48818545-48818905 | Common:1; Rare:126 | ||||
| chr12:48852083-48852322 | Common:2; Rare:76 | ||||
| chr12:48904114-48904149 | Rare:7 | ||||
| chr12:48939682-48940102 | Common:2; Rare:91 | ||||
| chr12:48957140-48957206 | Rare:13 | ||||
| chr12:48957367-48957688 | Common:4; Rare:86 |