| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:32583663-32583929 | Rare:95 | ||||
| chr11:33015792-33015935 | Common:1; Rare:57 | ||||
| chr11:33161400-33161682 | Common:6; Rare:77 | ||||
| chr11:33257152-33257441 | Common:3; Rare:101 | ||||
| chr11:33736391-33736612 | Common:2; Rare:70 | ||||
| chr11:34051617-34051732 | Rare:47 | ||||
| chr11:34052119-34052510 | Common:4; Rare:175 | ||||
| chr11:34105532-34105724 | Common:2; Rare:65 | ||||
| chr11:34916246-34916681 | Common:11; Rare:174; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35139018-35139275 | Common:1; Rare:58 | ||||
| chr11:35662580-35662945 | Common:3; Rare:115 | ||||
| chr11:35943901-35944121 | Common:3; Rare:71 | ||||
| chr11:36289372-36289505 | Common:1; Rare:54 | ||||
| chr11:36376262-36376541 | Common:3; Rare:56 | ||||
| chr11:36510229-36510361 | Rare:40 |