Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20684480-20684614 | Common:1; Rare:22; Clinvar (benign):1 | ||||
chr14:21437228-21437430 | Common:4; Rare:87 | ||||
chr14:21456060-21456238 | Common:2; Rare:53 | ||||
chr14:21476868-21477271 | Common:2; Rare:131 | ||||
chr14:21511284-21511553 | Rare:67 | ||||
chr14:22598143-22598303 | Common:1; Rare:54 | ||||
chr14:22766500-22766704 | Common:1; Rare:100 | ||||
chr14:22929363-22929609 | Rare:56 | ||||
chr14:22957029-22957241 | Common:1; Rare:62 | ||||
chr14:22982508-22982726 | Rare:84 | ||||
chr14:23095093-23095443 | Common:1; Rare:162 | ||||
chr14:23095452-23095594 | Common:2; Rare:53 | ||||
chr14:23306659-23306879 | Common:1; Rare:48 | ||||
chr14:24146555-24146881 | Common:1; Rare:104 | ||||
chr14:24195420-24195748 | Common:1; Rare:75 |