Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:114281548-114281684 | Common:1; Rare:82 | ||||
chr13:114281841-114282065 | Common:5; Rare:102 | ||||
chr14:20343186-20343644 | Common:12; Rare:269 | ||||
chr14:20413403-20413551 | Common:3; Rare:47 | ||||
chr14:20454762-20455320 | Common:7; Rare:145 | ||||
chr14:20683927-20684235 | Common:18; Rare:154; Clinvar:1; Clinvar (benign):1 | ||||
chr14:20684303-20684329 | Rare:5 | ||||
chr14:20684418-20684756 | Common:3; Rare:68; Clinvar:1; Clinvar (benign):3 | ||||
chr14:20802796-20802970 | Common:1; Rare:23 | ||||
chr14:21022100-21022435 | Rare:84 | ||||
chr14:21024997-21025309 | Rare:103 | ||||
chr14:21025456-21025554 | Common:1; Rare:24 | ||||
chr14:21025675-21025935 | Common:2; Rare:47 | ||||
chr14:21437232-21437414 | Common:4; Rare:73 | ||||
chr14:21456041-21456238 | Common:3; Rare:55 |