Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:100238568-100238831 | Common:2; Rare:78 | ||||
chr14:100376264-100376504 | Common:3; Rare:79 | ||||
chr14:101809792-101809887 | Rare:19 | ||||
chr14:102086986-102087434 | Common:5; Rare:193 | ||||
chr14:102139678-102139935 | Rare:90 | ||||
chr14:102362862-102363112 | Rare:108 | ||||
chr14:102928513-102928679 | Rare:56 | ||||
chr14:103333948-103334258 | Common:2; Rare:127 | ||||
chr14:103529070-103529240 | Common:1; Rare:52 | ||||
chr14:103562620-103563019 | Common:6; Rare:144; Clinvar (benign):2 | ||||
chr14:103715466-103715860 | Common:1; Rare:129 | ||||
chr14:104104652-104104978 | Common:1; Rare:97 | ||||
chr14:104970454-104970824 | Common:4; Rare:67 | ||||
chr14:105487015-105487205 | Common:1; Rare:47 | ||||
chr15:28099277-28099544 | Common:2; Rare:95; Clinvar:1 |