Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24195400-24195756 | Common:2; Rare:81 | ||||
chr14:24213441-24213539 | Rare:35 | ||||
chr14:24232289-24232680 | Common:8; Rare:102 | ||||
chr14:24232747-24232972 | Common:1; Rare:53 | ||||
chr14:24242272-24242431 | Rare:51; Clinvar (benign):2 | ||||
chr14:24271461-24271692 | Common:2; Rare:67 | ||||
chr14:24299738-24299862 | Common:4; Rare:34 | ||||
chr14:24429861-24429984 | Rare:28 | ||||
chr14:24442650-24443023 | Common:5; Rare:120 | ||||
chr14:25049890-25050193 | Common:3; Rare:94 | ||||
chr14:30559055-30559187 | Common:2; Rare:45 | ||||
chr14:31207647-31207911 | Common:2; Rare:93 | ||||
chr14:31420504-31420857 | Common:5; Rare:105 | ||||
chr14:32076134-32076290 | Rare:46 | ||||
chr14:32076688-32077051 | Common:3; Rare:110 |