| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:1040583-1040753 | Rare:36 | ||||
| chr11:1054410-1054760 | Common:9; Rare:167 | ||||
| chr11:1073290-1073720 | Common:4; Rare:137 | ||||
| chr11:1203653-1204220 | Common:6; Rare:247 | ||||
| chr11:1262650-1262880 | Common:7; Rare:124 | ||||
| chr11:1382820-1383290 | Common:4; Rare:241 | ||||
| chr11:1547142-1547550 | Common:8; Rare:196 | ||||
| chr11:1548350-1548720 | Common:1; Rare:83 | ||||
| chr11:1558120-1558720 | Common:5; Rare:181 | ||||
| chr11:1572930-1573300 | Common:20; Rare:135 | ||||
| chr11:1753486-1754393 | Common:9; Rare:473; Clinvar:26; Clinvar (benign):49; Clinvar (pathogenic):4 | ||||
| chr11:1773529-1773762 | Common:2; Rare:72 | ||||
| chr11:2377960-2378170 | Common:7; Rare:95 | ||||
| chr11:2892290-2892820 | Common:2; Rare:257 | ||||
| chr11:2898670-2898980 | Common:6; Rare:70 |