Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103562624-103563013 | Common:6; Rare:139; Clinvar (benign):2 | ||||
chr15:23039540-23039703 | Common:1; Rare:64 | ||||
chr15:30903706-30903936 | Common:1; Rare:56 | ||||
chr15:32615386-32615566 | Common:3; Rare:45 | ||||
chr15:33194707-33194923 | Common:1; Rare:61 | ||||
chr15:34101843-34102083 | Common:1; Rare:48 | ||||
chr15:35546148-35546280 | Common:1; Rare:46 | ||||
chr15:37100506-37100775 | Common:1; Rare:91 | ||||
chr15:39782794-39782877 | Rare:22 | ||||
chr15:40039096-40039329 | Rare:98 | ||||
chr15:40695075-40695167 | Rare:25 | ||||
chr15:40807436-40807761 | Common:4; Rare:107 | ||||
chr15:40843843-40844057 | Common:2; Rare:65 | ||||
chr15:40844356-40844629 | Rare:99 | ||||
chr15:41402456-41402554 | Common:2; Rare:30 |