| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr11:74085510-74085810 | Common:3; Rare:125 | ||||
| chr11:74090693-74091093 | Common:1; Rare:133 | ||||
| chr11:74170810-74171438 | Common:25; Rare:1259 | ||||
| chr11:74171726-74172135 | Common:4; Rare:131 | ||||
| chr11:74397536-74397936 | Common:4; Rare:69 | ||||
| chr11:74398301-74399045 | Common:18; Rare:762 | ||||
| chr11:74461718-74462460 | Common:9; Rare:178 | ||||
| chr11:74467404-74467804 | Common:9; Rare:135; Clinvar (benign):1 | ||||
| chr11:74492910-74493414 | Common:7; Rare:748; Clinvar (pathogenic):6 | ||||
| chr11:74493635-74494035 | Common:6; Rare:378 | ||||
| chr11:74592259-74592744 | Common:5; Rare:404 | ||||
| chr11:74592749-74593171 | Common:4; Rare:165 | ||||
| chr11:74748570-74748986 | Common:14; Rare:442 | ||||
| chr11:74749180-74749890 | Common:9; Rare:243 | ||||
| chr11:74948985-74949756 | Common:51; Rare:806 |