Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:69398251-69398426 | Common:1; Rare:69 | ||||
chr14:69398612-69398723 | Rare:29 | ||||
chr14:69611480-69611708 | Common:1; Rare:78 | ||||
chr14:70416998-70417124 | Rare:36 | ||||
chr14:71320296-71320485 | Rare:59 | ||||
chr14:71320888-71321164 | Common:3; Rare:92 | ||||
chr14:72926164-72926516 | Common:6; Rare:87 | ||||
chr14:73058309-73058579 | Common:3; Rare:79 | ||||
chr14:73458513-73458849 | Common:5; Rare:86 | ||||
chr14:73569052-73569292 | Rare:57 | ||||
chr14:73592049-73592139 | Common:2; Rare:29 | ||||
chr14:73644885-73645037 | Common:2; Rare:41; Clinvar:2 | ||||
chr14:73787133-73787359 | Common:2; Rare:82 | ||||
chr14:73851621-73851957 | Common:2; Rare:94 | ||||
chr14:73950080-73950328 | Common:5; Rare:100; Clinvar (benign):3 |