| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:18322123-18322308 | Common:3; Rare:67; Clinvar:1; Clinvar (benign):2 | ||||
| chr11:18322492-18322584 | Common:2; Rare:40 | ||||
| chr11:18526851-18526985 | Rare:66 | ||||
| chr11:18588656-18588916 | Common:3; Rare:91 | ||||
| chr11:18634291-18634546 | Common:3; Rare:90 | ||||
| chr11:20363683-20363793 | Common:2; Rare:24 | ||||
| chr11:27506720-27506859 | Common:1; Rare:66 | ||||
| chr11:28108146-28108396 | Common:1; Rare:70 | ||||
| chr11:30322949-30323162 | Common:1; Rare:59 | ||||
| chr11:31369737-31369903 | Rare:52 | ||||
| chr11:31509589-31509787 | Common:1; Rare:62 | ||||
| chr11:32435389-32435733 | Common:1; Rare:75; Clinvar:4 | ||||
| chr11:33015795-33015895 | Rare:38 | ||||
| chr11:33161449-33161674 | Common:6; Rare:61 | ||||
| chr11:34916280-34916578 | Common:8; Rare:124; Clinvar:5; Clinvar (benign):8; Clinvar (pathogenic):1 |