| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:86955396-86955645 | Common:1; Rare:72 | ||||
| chr11:87037792-87038063 | Common:2; Rare:126 | ||||
| chr11:88337634-88337894 | Common:4; Rare:124; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:90222982-90223231 | Common:2; Rare:97 | ||||
| chr11:93741374-93741716 | Common:7; Rare:136 | ||||
| chr11:93784165-93784336 | Common:2; Rare:64 | ||||
| chr11:94493789-94494031 | Common:3; Rare:68; Clinvar (benign):1 | ||||
| chr11:94768185-94768399 | Common:1; Rare:65 | ||||
| chr11:94973497-94973711 | Rare:71 | ||||
| chr11:95067473-95067573 | Rare:35 | ||||
| chr11:95089729-95089930 | Common:3; Rare:87 | ||||
| chr11:95789555-95789870 | Common:3; Rare:141 | ||||
| chr11:95790353-95790704 | Common:3; Rare:135 | ||||
| chr11:95923829-95924157 | Common:2; Rare:145; Clinvar:5; Clinvar (benign):5 | ||||
| chr11:96389846-96390061 | Common:1; Rare:93 |