Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20684438-20684599 | Common:2; Rare:26; Clinvar (benign):2 | ||||
chr14:20989960-20990032 | Common:2; Rare:34 | ||||
chr14:21211553-21211882 | Common:3; Rare:84 | ||||
chr14:21383948-21384283 | Common:8; Rare:107 | ||||
chr14:21476849-21477267 | Common:2; Rare:138 | ||||
chr14:21511238-21511551 | Rare:94 | ||||
chr14:22589155-22589479 | Common:4; Rare:103 | ||||
chr14:22766512-22766746 | Common:1; Rare:130 | ||||
chr14:22871454-22871949 | Rare:116 | ||||
chr14:22919077-22919456 | Common:8; Rare:101 | ||||
chr14:22929341-22929634 | Common:1; Rare:80 | ||||
chr14:23064112-23064398 | Rare:67 | ||||
chr14:23095442-23095567 | Common:2; Rare:52 | ||||
chr14:23302756-23302958 | Rare:37 | ||||
chr14:23306626-23306899 | Common:1; Rare:60 |