| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:33161303-33161767 | Common:7; Rare:124 | ||||
| chr11:33257157-33257427 | Common:3; Rare:92 | ||||
| chr11:33736392-33736621 | Common:2; Rare:74 | ||||
| chr11:33774500-33774670 | Common:2; Rare:62 | ||||
| chr11:34051617-34051761 | Rare:61 | ||||
| chr11:34052119-34052364 | Common:2; Rare:107 | ||||
| chr11:34053492-34053544 | Rare:15 | ||||
| chr11:34105481-34105760 | Common:2; Rare:91 | ||||
| chr11:34438776-34439009 | Common:2; Rare:79; Clinvar (benign):1 | ||||
| chr11:34916242-34916694 | Common:11; Rare:183; Clinvar:6; Clinvar (benign):12; Clinvar (pathogenic):1 | ||||
| chr11:35419556-35419701 | Rare:27 | ||||
| chr11:35420203-35420300 | Rare:15 | ||||
| chr11:35662687-35662925 | Common:2; Rare:73 | ||||
| chr11:35943917-35944135 | Common:3; Rare:71 | ||||
| chr11:36289320-36289505 | Common:2; Rare:66 |