| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1573900-1574510 | Common:6; Rare:177 | ||||
| chr11:1589233-1589663 | Common:4; Rare:118 | ||||
| chr11:1693858-1693989 | Common:1; Rare:36 | ||||
| chr11:1705501-1706020 | Common:6; Rare:259 | ||||
| chr11:1742430-1743080 | Common:5; Rare:124 | ||||
| chr11:1747943-1748366 | Common:2; Rare:131 | ||||
| chr11:1753470-1754070 | Common:8; Rare:474; Clinvar:30; Clinvar (benign):54; Clinvar (pathogenic):4 | ||||
| chr11:1781380-1781860 | Common:6; Rare:160 | ||||
| chr11:1782837-1783243 | Common:8; Rare:175 | ||||
| chr11:1796400-1797120 | Common:5; Rare:263 | ||||
| chr11:1827150-1827580 | Common:8; Rare:264 | ||||
| chr11:1943836-1944313 | Common:5; Rare:189 | ||||
| chr11:2190782-2191047 | Common:1; Rare:66 | ||||
| chr11:2191080-2191560 | Common:14; Rare:187 | ||||
| chr11:2191855-2192632 | Common:18; Rare:276 |