| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:117986270-117986418 | Common:4; Rare:50; Clinvar:2 | ||||
| chr11:118264283-118264593 | Common:1; Rare:50 | ||||
| chr11:118359451-118359667 | Common:3; Rare:92 | ||||
| chr11:118401295-118401698 | Rare:133 | ||||
| chr11:118572331-118572463 | Common:2; Rare:48 | ||||
| chr11:118607316-118607638 | Common:2; Rare:44 | ||||
| chr11:118621215-118621498 | Rare:59 | ||||
| chr11:118790869-118791263 | Rare:115 | ||||
| chr11:118997980-118998193 | Common:4; Rare:66 | ||||
| chr11:119018280-119018538 | Common:8; Rare:110 | ||||
| chr11:119018635-119018798 | Common:5; Rare:71 | ||||
| chr11:119057120-119057448 | Common:3; Rare:131 | ||||
| chr11:119067736-119067821 | Rare:31 | ||||
| chr11:119121273-119121626 | Common:1; Rare:83 | ||||
| chr11:119206180-119206373 | Common:5; Rare:87; Clinvar:7; Clinvar (benign):4 |