Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr14:103562611-103563024 | Common:6; Rare:151; Clinvar (benign):2 | ||||
chr14:103715434-103715842 | Common:1; Rare:133 | ||||
chr14:105248442-105248554 | Common:1; Rare:33 | ||||
chr15:22786516-22786659 | Rare:39; Clinvar:1 | ||||
chr15:25863340-25863479 | Common:2; Rare:36 | ||||
chr15:29822431-29822648 | Common:2; Rare:90 | ||||
chr15:30903694-30903942 | Common:1; Rare:63 | ||||
chr15:34101829-34102117 | Common:1; Rare:62 | ||||
chr15:35546142-35546180 | Rare:12 | ||||
chr15:37100337-37100677 | Common:1; Rare:89 | ||||
chr15:39581058-39581194 | Common:2; Rare:43 | ||||
chr15:39581198-39581503 | Rare:61 | ||||
chr15:39588122-39588712 | Common:4; Rare:150; Clinvar (benign):3 | ||||
chr15:39588919-39589352 | Common:1; Rare:136 | ||||
chr15:39591164-39591526 | Rare:91 |