Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:59484315-59484570 | Common:3; Rare:102 | ||||
chr14:60981045-60981308 | Common:1; Rare:96 | ||||
chr14:63641839-63642071 | Common:3; Rare:74 | ||||
chr14:64387992-64388413 | Common:2; Rare:154 | ||||
chr14:64503656-64503887 | Common:2; Rare:89 | ||||
chr14:64504572-64504817 | Rare:68 | ||||
chr14:65412564-65412806 | Common:1; Rare:76 | ||||
chr14:67359761-67360006 | Rare:75 | ||||
chr14:69398310-69398707 | Common:2; Rare:99 | ||||
chr14:70417025-70417124 | Rare:25 | ||||
chr14:73058358-73058603 | Common:3; Rare:80 | ||||
chr14:73886818-73886877 | Rare:18 | ||||
chr14:73950134-73950358 | Common:3; Rare:105; Clinvar (benign):1 | ||||
chr14:74019262-74019452 | Common:1; Rare:70 | ||||
chr14:74493570-74493777 | Common:3; Rare:78; Clinvar (benign):4 |