| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118264271-118264643 | Common:1; Rare:54 | ||||
| chr11:118344323-118344414 | Common:1; Rare:18; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:118401330-118401704 | Rare:127 | ||||
| chr11:118610370-118610440 | Rare:13 | ||||
| chr11:118621281-118621498 | Rare:45 | ||||
| chr11:118790875-118791297 | Rare:139 | ||||
| chr11:118910487-118910681 | Common:3; Rare:63 | ||||
| chr11:118997980-118998287 | Common:4; Rare:102 | ||||
| chr11:119018280-119018457 | Common:6; Rare:72 | ||||
| chr11:119018626-119018808 | Common:5; Rare:75 | ||||
| chr11:119057045-119057456 | Common:3; Rare:155 | ||||
| chr11:119067624-119067866 | Common:3; Rare:79 | ||||
| chr11:119101767-119101947 | Rare:50; Clinvar:2 | ||||
| chr11:119107621-119107897 | Common:1; Rare:73 | ||||
| chr11:119110624-119110927 | Rare:81 |