| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33257295-33257493 | Common:2; Rare:61 | ||||
| chr11:33257585-33257793 | Rare:50 | ||||
| chr11:33257802-33257876 | Common:1; Rare:19 | ||||
| chr11:33258181-33258626 | Common:2; Rare:168 | ||||
| chr11:33736376-33736605 | Common:2; Rare:72 | ||||
| chr11:33774457-33774670 | Common:2; Rare:79 | ||||
| chr11:34052062-34052536 | Common:5; Rare:207 | ||||
| chr11:34105462-34105730 | Common:3; Rare:90 | ||||
| chr11:34438784-34439027 | Common:2; Rare:85; Clinvar (benign):1 | ||||
| chr11:34916287-34916494 | Common:4; Rare:85; Clinvar:3; Clinvar (benign):4; Clinvar (pathogenic):1 | ||||
| chr11:34916501-34916676 | Common:6; Rare:69; Clinvar:1; Clinvar (benign):7 | ||||
| chr11:35139018-35139369 | Common:1; Rare:96 | ||||
| chr11:35663018-35663339 | Rare:107 | ||||
| chr11:35943804-35944125 | Common:3; Rare:104 | ||||
| chr11:36510229-36510377 | Rare:45 |