| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:828878-829278 | Common:5; Rare:257 | ||||
| chr11:832804-833020 | Common:7; Rare:71 | ||||
| chr11:842540-842970 | Common:8; Rare:160 | ||||
| chr11:843825-844554 | Common:5; Rare:241 | ||||
| chr11:844706-845106 | Common:7; Rare:145 | ||||
| chr11:849630-849970 | Common:5; Rare:131 | ||||
| chr11:910791-910925 | Common:3; Rare:48 | ||||
| chr11:925869-926711 | Common:1; Rare:312 | ||||
| chr11:946050-946390 | Common:4; Rare:68 | ||||
| chr11:1309581-1309929 | Common:3; Rare:128 | ||||
| chr11:1389747-1390112 | Common:5; Rare:84 | ||||
| chr11:1390327-1391139 | Common:4; Rare:241 | ||||
| chr11:1572262-1572383 | Rare:34 | ||||
| chr11:1763896-1764097 | Common:3; Rare:85; Clinvar:3; Clinvar (benign):2 | ||||
| chr11:1830626-1831026 | Common:1; Rare:168 |