Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103715466-103715853 | Common:1; Rare:126 | ||||
chr14:104579576-104579811 | Common:1; Rare:51 | ||||
chr14:104689509-104689664 | Rare:36 | ||||
chr14:104753116-104753295 | Common:1; Rare:80 | ||||
chr14:104773258-104773491 | Rare:54; Clinvar:4; Clinvar (benign):5 | ||||
chr15:22838356-22838717 | Common:3; Rare:129 | ||||
chr15:24954918-24955004 | Rare:45 | ||||
chr15:25438984-25439175 | Common:2; Rare:70 | ||||
chr15:28738399-28738517 | Common:1; Rare:21 | ||||
chr15:29269792-29269878 | Rare:32 | ||||
chr15:30903732-30903969 | Common:1; Rare:64 | ||||
chr15:31365963-31366133 | Common:2; Rare:44 | ||||
chr15:32615096-32615580 | Common:6; Rare:124 | ||||
chr15:34101634-34101658 | Rare:4 | ||||
chr15:34101836-34102131 | Common:1; Rare:63 |