Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:49586331-49586778 | Common:1; Rare:240 | ||||
chr14:49598731-49599041 | Common:1; Rare:114 | ||||
chr14:49620563-49620835 | Common:2; Rare:113; Clinvar:3 | ||||
chr14:49688193-49688287 | Rare:37 | ||||
chr14:49892913-49893136 | Rare:91 | ||||
chr14:50312189-50312392 | Common:1; Rare:82 | ||||
chr14:50396874-50397022 | Common:2; Rare:46 | ||||
chr14:50561118-50561149 | Rare:8 | ||||
chr14:50668322-50668556 | Common:3; Rare:86 | ||||
chr14:50944373-50944616 | Common:4; Rare:85; Clinvar:1; Clinvar (benign):2 | ||||
chr14:51240107-51240291 | Common:1; Rare:77 | ||||
chr14:51651646-51652043 | Common:4; Rare:115 | ||||
chr14:51860549-51860774 | Rare:65 | ||||
chr14:51989374-51989664 | Common:2; Rare:93 | ||||
chr14:52003940-52004221 | Common:2; Rare:92 |