| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:110712344-110712584 | Common:2; Rare:83 | ||||
| chr11:111364295-111364440 | Rare:24 | ||||
| chr11:111378687-111378902 | Common:3; Rare:42 | ||||
| chr11:111379100-111379325 | Rare:56 | ||||
| chr11:111379326-111379504 | Common:2; Rare:38 | ||||
| chr11:111379592-111380053 | Common:4; Rare:81 | ||||
| chr11:111398321-111398517 | Rare:29 | ||||
| chr11:111601995-111602109 | Rare:22 | ||||
| chr11:111602239-111602497 | Common:1; Rare:86 | ||||
| chr11:111766095-111766159 | Common:2; Rare:21 | ||||
| chr11:111766290-111766522 | Common:3; Rare:126 | ||||
| chr11:111871114-111871432 | Common:5; Rare:84; Clinvar:1 | ||||
| chr11:111871455-111871673 | Rare:75; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:111878297-111878468 | Rare:30 | ||||
| chr11:111878897-111879346 | Common:2; Rare:186 |