| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr12:109477868-109477908 | Rare:12 | ||||
| chr12:109519256-109519468 | Common:1; Rare:42 | ||||
| chr12:109573116-109573367 | Common:2; Rare:66 | ||||
| chr12:109573429-109573858 | Common:3; Rare:139; Clinvar:7; Clinvar (benign):5; Clinvar (pathogenic):2 | ||||
| chr12:109713814-109713985 | Common:2; Rare:62 | ||||
| chr12:109880423-109880684 | Common:1; Rare:70 | ||||
| chr12:109900109-109900377 | Rare:81 | ||||
| chr12:109900494-109900748 | Common:1; Rare:54 | ||||
| chr12:109900800-109900886 | Rare:18 | ||||
| chr12:109901043-109901172 | Common:1; Rare:25 | ||||
| chr12:109996213-109996494 | Common:2; Rare:83 | ||||
| chr12:109999038-109999471 | Rare:97 | ||||
| chr12:109999565-109999647 | Rare:11 | ||||
| chr12:110048453-110048796 | Common:2; Rare:84 | ||||
| chr12:110124088-110124517 | Common:2; Rare:126 |