| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:575786-576241 | Common:14; Rare:286 | ||||
| chr11:576374-576537 | Rare:138 | ||||
| chr11:615650-615830 | Common:2; Rare:108 | ||||
| chr11:615900-616136 | Common:3; Rare:150 | ||||
| chr11:693482-693901 | Common:6; Rare:194 | ||||
| chr11:694594-694761 | Rare:84 | ||||
| chr11:694958-695427 | Common:3; Rare:350; Clinvar:3 | ||||
| chr11:695696-695878 | Common:6; Rare:176 | ||||
| chr11:704954-705285 | Common:3; Rare:173 | ||||
| chr11:705918-706309 | Common:8; Rare:315 | ||||
| chr11:706921-707321 | Common:3; Rare:90 | ||||
| chr11:747180-747540 | Rare:345; Clinvar:7; Clinvar (benign):3 | ||||
| chr11:747713-748301 | Common:2; Rare:161 | ||||
| chr11:777396-777694 | Common:5; Rare:299 | ||||
| chr11:797430-797795 | Rare:164 |