| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:3855535-3855729 | Common:2; Rare:40 | ||||
| chr11:3855898-3856193 | Rare:79 | ||||
| chr11:4393634-4393779 | Common:1; Rare:33 | ||||
| chr11:5624897-5625034 | Rare:20 | ||||
| chr11:6390241-6390502 | Common:2; Rare:74 | ||||
| chr11:6390794-6390913 | Rare:47; Clinvar:5; Clinvar (benign):1; Clinvar (pathogenic):2 | ||||
| chr11:6391279-6391440 | Common:1; Rare:51; Clinvar:7; Clinvar (pathogenic):1 | ||||
| chr11:6481261-6481562 | Common:5; Rare:132 | ||||
| chr11:6603448-6603831 | Common:4; Rare:126; Clinvar (benign):3 | ||||
| chr11:7513616-7513991 | Common:6; Rare:116 | ||||
| chr11:7648216-7648537 | Rare:88 | ||||
| chr11:7649662-7649781 | Common:1; Rare:16 | ||||
| chr11:7672813-7672955 | Rare:60 | ||||
| chr11:7673442-7673534 | Common:1; Rare:28 | ||||
| chr11:7674185-7674263 | Common:1; Rare:29 |