| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:126355514-126355785 | Common:2; Rare:77 | ||||
| chr11:128522263-128522521 | Common:1; Rare:81 | ||||
| chr11:128694064-128694154 | Rare:18 | ||||
| chr11:130069626-130069976 | Common:2; Rare:128 | ||||
| chr11:130314403-130314457 | Rare:22 | ||||
| chr11:131911302-131911444 | Common:1; Rare:48 | ||||
| chr11:134224533-134224695 | Rare:61 | ||||
| chr11:134253298-134253594 | Common:2; Rare:98; Clinvar (benign):1 | ||||
| chr12:389238-389383 | Rare:56 | ||||
| chr12:401446-401677 | Rare:61 | ||||
| chr12:643624-643941 | Common:2; Rare:65 | ||||
| chr12:752347-752597 | Common:1; Rare:74 | ||||
| chr12:949516-949609 | Common:3; Rare:24 | ||||
| chr12:990471-990576 | Common:1; Rare:31 | ||||
| chr12:991085-991322 | Common:4; Rare:106 |