| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:10808887-10809043 | Rare:70 | ||||
| chr11:10858010-10858260 | Common:3; Rare:82 | ||||
| chr11:11841941-11842079 | Common:1; Rare:38 | ||||
| chr11:12161079-12161503 | Common:3; Rare:72 | ||||
| chr11:12473815-12473935 | Rare:36 | ||||
| chr11:13463150-13463548 | Common:2; Rare:129 | ||||
| chr11:14643627-14643699 | Common:1; Rare:33 | ||||
| chr11:16738464-16738862 | Common:3; Rare:96 | ||||
| chr11:17207868-17208061 | Common:2; Rare:70 | ||||
| chr11:18322091-18322332 | Common:5; Rare:92; Clinvar:2; Clinvar (benign):2 | ||||
| chr11:18322482-18322637 | Common:2; Rare:67 | ||||
| chr11:18394461-18394634 | Common:1; Rare:69; Clinvar (benign):1 | ||||
| chr11:18526841-18526977 | Rare:66 | ||||
| chr11:18588667-18588884 | Common:2; Rare:74 | ||||
| chr11:18634232-18634493 | Common:2; Rare:96 |