| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:118401329-118401672 | Rare:114 | ||||
| chr11:118572336-118572447 | Common:2; Rare:38 | ||||
| chr11:118572724-118572793 | Common:1; Rare:12 | ||||
| chr11:118610143-118610440 | Rare:40 | ||||
| chr11:118621134-118621521 | Rare:77 | ||||
| chr11:118790894-118791320 | Common:1; Rare:146 | ||||
| chr11:118910376-118910683 | Common:3; Rare:93 | ||||
| chr11:118997956-118998206 | Common:4; Rare:83 | ||||
| chr11:119018280-119018823 | Common:13; Rare:209 | ||||
| chr11:119057048-119057448 | Common:3; Rare:153 | ||||
| chr11:119067624-119067843 | Common:3; Rare:71 | ||||
| chr11:119101797-119101947 | Rare:44; Clinvar:2 | ||||
| chr11:119121279-119121626 | Common:1; Rare:79 | ||||
| chr11:119206175-119206396 | Common:5; Rare:99; Clinvar:8; Clinvar (benign):4 | ||||
| chr11:119311371-119311848 | Common:1; Rare:146 |