| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:11841859-11842079 | Common:2; Rare:74 | ||||
| chr11:13463168-13463367 | Common:1; Rare:75 | ||||
| chr11:14499783-14499922 | Common:2; Rare:47 | ||||
| chr11:14520314-14520520 | Rare:67 | ||||
| chr11:16738450-16738736 | Common:3; Rare:65 | ||||
| chr11:17077608-17077854 | Common:2; Rare:102 | ||||
| chr11:17207911-17208078 | Common:2; Rare:64 | ||||
| chr11:17276540-17276818 | Common:4; Rare:81; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr11:18012903-18013047 | Common:4; Rare:55 | ||||
| chr11:18106037-18106160 | Common:1; Rare:56 | ||||
| chr11:18322158-18322317 | Common:1; Rare:52 | ||||
| chr11:18322508-18322631 | Common:2; Rare:56 | ||||
| chr11:18394397-18394623 | Common:1; Rare:92; Clinvar (benign):1 | ||||
| chr11:18396204-18396408 | Rare:75 | ||||
| chr11:18526847-18526993 | Rare:71 |