Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:63543312-63543626 | Common:4; Rare:88 | ||||
chr14:65102442-65102839 | Common:8; Rare:105; Clinvar:1; Clinvar (benign):1 | ||||
chr14:67359765-67360030 | Rare:87 | ||||
chr14:67360062-67360402 | Common:4; Rare:89 | ||||
chr14:67619717-67619962 | Common:1; Rare:61 | ||||
chr14:67816578-67816720 | Rare:25 | ||||
chr14:68979199-68979532 | Common:2; Rare:98 | ||||
chr14:69191421-69191548 | Rare:25 | ||||
chr14:69398237-69398419 | Rare:73 | ||||
chr14:69398581-69398714 | Rare:32 | ||||
chr14:70416977-70417131 | Rare:47 | ||||
chr14:70600635-70600880 | Common:2; Rare:59 | ||||
chr14:71320328-71320466 | Rare:41 | ||||
chr14:73058301-73058583 | Common:3; Rare:84 | ||||
chr14:73458526-73458870 | Common:5; Rare:90 |