| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:17353624-17353840 | Common:5; Rare:66 | ||||
| chr11:17405410-17406160 | Common:5; Rare:163; Clinvar:1; Clinvar (benign):1 | ||||
| chr11:17473488-17473645 | Common:2; Rare:30 | ||||
| chr11:17479665-17479780 | Rare:19 | ||||
| chr11:17649890-17650330 | Common:2; Rare:77 | ||||
| chr11:17650350-17650730 | Common:3; Rare:78 | ||||
| chr11:17683080-17683580 | Common:2; Rare:78 | ||||
| chr11:17722030-17722310 | Rare:70 | ||||
| chr11:17730940-17731310 | Common:2; Rare:64 | ||||
| chr11:17786929-17787097 | Rare:36 | ||||
| chr11:18383694-18384019 | Common:2; Rare:57 | ||||
| chr11:18384260-18384466 | Rare:34 | ||||
| chr11:18668488-18668888 | Common:7; Rare:141 | ||||
| chr11:18669339-18669537 | Common:2; Rare:25 | ||||
| chr11:18721137-18721355 | Rare:47 |