Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:20455039-20455287 | Common:2; Rare:74 | ||||
chr14:20683976-20684345 | Common:18; Rare:167; Clinvar:2; Clinvar (benign):3 | ||||
chr14:20684461-20684739 | Common:2; Rare:53; Clinvar:1; Clinvar (benign):2 | ||||
chr14:20802795-20802973 | Common:1; Rare:23 | ||||
chr14:21025023-21025191 | Rare:60 | ||||
chr14:21025680-21025885 | Common:2; Rare:35 | ||||
chr14:21383938-21384083 | Common:1; Rare:55 | ||||
chr14:21456041-21456353 | Common:4; Rare:80 | ||||
chr14:21476868-21477267 | Common:2; Rare:128 | ||||
chr14:21511284-21511534 | Rare:64 | ||||
chr14:21526279-21526460 | Rare:36 | ||||
chr14:22766560-22766700 | Common:1; Rare:74 | ||||
chr14:22829778-22829915 | Rare:48 | ||||
chr14:22871651-22872230 | Common:2; Rare:143 | ||||
chr14:22919121-22919456 | Common:7; Rare:81 |