Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:67241133-67241442 | Rare:76 | ||||
chr14:67359738-67360023 | Common:1; Rare:91 | ||||
chr14:67360263-67360404 | Common:2; Rare:48 | ||||
chr14:67619704-67619881 | Common:1; Rare:37 | ||||
chr14:67674584-67674933 | Common:1; Rare:85 | ||||
chr14:68793049-68793369 | Common:1; Rare:67 | ||||
chr14:68979188-68979539 | Common:2; Rare:106 | ||||
chr14:69398248-69398731 | Common:2; Rare:145 | ||||
chr14:70417025-70417124 | Rare:25 | ||||
chr14:71320267-71320491 | Rare:70 | ||||
chr14:71320899-71321164 | Common:3; Rare:88 | ||||
chr14:73463588-73463813 | Common:1; Rare:39 | ||||
chr14:73569240-73569309 | Rare:26 | ||||
chr14:73851705-73851976 | Common:4; Rare:90 | ||||
chr14:73950113-73950323 | Common:5; Rare:79; Clinvar (benign):3 |