Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:24146582-24146693 | Rare:40 | ||||
chr14:24195418-24195711 | Common:1; Rare:67 | ||||
chr14:24232312-24232673 | Common:8; Rare:88 | ||||
chr14:24232847-24232953 | Rare:24 | ||||
chr14:24242580-24242743 | Common:1; Rare:33; Clinvar:1; Clinvar (benign):2 | ||||
chr14:24299714-24299858 | Common:4; Rare:42 | ||||
chr14:24429855-24429980 | Rare:30 | ||||
chr14:24442755-24443017 | Common:5; Rare:76 | ||||
chr14:25049901-25050208 | Common:2; Rare:96 | ||||
chr14:30559047-30559178 | Common:2; Rare:45 | ||||
chr14:31420543-31420763 | Common:2; Rare:66 | ||||
chr14:31457369-31457577 | Common:2; Rare:73 | ||||
chr14:31561328-31561450 | Common:2; Rare:49; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
chr14:32076664-32077045 | Common:3; Rare:114 | ||||
chr14:34462230-34462540 | Common:1; Rare:103 |