Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:64987105-64987231 | Rare:50 | ||||
chr14:66508460-66508521 | Rare:31 | ||||
chr14:67241117-67241423 | Rare:78 | ||||
chr14:67359773-67360031 | Rare:87 | ||||
chr14:67360268-67360368 | Common:1; Rare:31 | ||||
chr14:67816578-67816708 | Rare:22 | ||||
chr14:69398253-69398403 | Rare:60 | ||||
chr14:69398595-69398723 | Rare:31 | ||||
chr14:69611480-69611732 | Common:1; Rare:83 | ||||
chr14:70416947-70417140 | Rare:61 | ||||
chr14:71321775-71321819 | Common:1; Rare:10 | ||||
chr14:73787133-73787373 | Common:2; Rare:86 | ||||
chr14:73886801-73886876 | Rare:20 | ||||
chr14:73950077-73950335 | Common:6; Rare:106; Clinvar (benign):4 | ||||
chr14:74019263-74019427 | Common:1; Rare:64 |