Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:21511145-21511561 | Rare:118 | ||||
chr14:21525639-21525784 | Common:1; Rare:32; Clinvar (pathogenic):1 | ||||
chr14:21526186-21526617 | Rare:85 | ||||
chr14:21536873-21537258 | Common:1; Rare:93 | ||||
chr14:22588962-22589274 | Common:2; Rare:95 | ||||
chr14:22766462-22766767 | Common:2; Rare:165 | ||||
chr14:22819753-22819885 | Common:2; Rare:28 | ||||
chr14:22836212-22836649 | Common:5; Rare:96 | ||||
chr14:22871477-22871852 | Rare:83 | ||||
chr14:22872592-22872785 | Common:1; Rare:62 | ||||
chr14:22883047-22883224 | Common:10; Rare:34 | ||||
chr14:22904887-22905117 | Rare:75 | ||||
chr14:22919078-22919456 | Common:8; Rare:101 | ||||
chr14:22929219-22929634 | Common:1; Rare:119 | ||||
chr14:22956962-22957193 | Common:1; Rare:64 |