| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322482-18322631 | Common:2; Rare:64 | ||||
| chr11:18394363-18394632 | Common:1; Rare:111; Clinvar (benign):1 | ||||
| chr11:18526851-18526957 | Rare:52 | ||||
| chr11:18634313-18634574 | Common:2; Rare:84 | ||||
| chr11:20387505-20387738 | Common:4; Rare:71 | ||||
| chr11:27506725-27506875 | Common:1; Rare:70 | ||||
| chr11:28108096-28108417 | Common:1; Rare:94 | ||||
| chr11:31509575-31509790 | Common:1; Rare:67 | ||||
| chr11:33015784-33015942 | Common:1; Rare:60 | ||||
| chr11:33161440-33161682 | Common:6; Rare:68 | ||||
| chr11:33722721-33722844 | Common:1; Rare:22 | ||||
| chr11:33736400-33736562 | Common:1; Rare:56 | ||||
| chr11:34438759-34439009 | Common:2; Rare:82; Clinvar (benign):1 | ||||
| chr11:34916287-34916658 | Common:10; Rare:150; Clinvar:5; Clinvar (benign):11; Clinvar (pathogenic):1 | ||||
| chr11:35138940-35139179 | Common:1; Rare:56 |