Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:22875084-22875402 | Common:1; Rare:87 | ||||
chr14:22929349-22929609 | Rare:60 | ||||
chr14:22976643-22976999 | Rare:73 | ||||
chr14:22982515-22982910 | Common:2; Rare:137 | ||||
chr14:23095093-23095594 | Common:3; Rare:221 | ||||
chr14:23286096-23286358 | Rare:55 | ||||
chr14:23306631-23306885 | Common:1; Rare:55 | ||||
chr14:23321817-23322035 | Common:2; Rare:61 | ||||
chr14:23555933-23556052 | Rare:32 | ||||
chr14:23556208-23556348 | Common:2; Rare:31 | ||||
chr14:23567728-23567862 | Rare:26 | ||||
chr14:23953605-23953896 | Common:10; Rare:118 | ||||
chr14:23988830-23988950 | Common:4; Rare:52 | ||||
chr14:24094013-24094432 | Common:4; Rare:114; Clinvar (benign):1 | ||||
chr14:24114445-24114848 | Common:1; Rare:95 |