| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:14520059-14520560 | Common:1; Rare:144 | ||||
| chr11:14643619-14643887 | Common:1; Rare:97 | ||||
| chr11:16738466-16738698 | Common:3; Rare:49 | ||||
| chr11:16738700-16738923 | Rare:66 | ||||
| chr11:16739453-16739784 | Common:1; Rare:67 | ||||
| chr11:17014194-17014332 | Rare:50 | ||||
| chr11:17014394-17014526 | Common:1; Rare:70 | ||||
| chr11:17207862-17208078 | Common:2; Rare:77 | ||||
| chr11:17276484-17276840 | Common:5; Rare:101; Clinvar:4; Clinvar (pathogenic):1 | ||||
| chr11:17311879-17312116 | Rare:50 | ||||
| chr11:17544387-17544497 | Common:2; Rare:29 | ||||
| chr11:18105790-18106120 | Common:3; Rare:131 | ||||
| chr11:18322079-18322306 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322476-18322735 | Common:2; Rare:92 | ||||
| chr11:18394418-18394644 | Common:1; Rare:88; Clinvar (benign):1 |