Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:143384198-143384617 | Common:3; Rare:64 | ||||
chr7:143386464-143386738 | Common:3; Rare:56 | ||||
chr7:148783818-148783977 | Common:1; Rare:47 | ||||
chr7:148807126-148807415 | Common:1; Rare:77; Clinvar (benign):1 | ||||
chr7:148816602-148816748 | Common:1; Rare:34; Clinvar:1; Clinvar (benign):2 | ||||
chr7:148987246-148987513 | Common:8; Rare:87 | ||||
chr7:149176225-149176547 | Common:2; Rare:63 | ||||
chr7:149210428-149210682 | Rare:58 | ||||
chr7:149255552-149255759 | Rare:46 | ||||
chr7:149839639-149839901 | Common:2; Rare:39 | ||||
chr7:149839983-149840085 | Rare:25 | ||||
chr7:149842737-149842802 | Rare:13 | ||||
chr7:151053973-151054231 | Rare:64 | ||||
chr7:151113363-151113672 | Common:1; Rare:60 | ||||
chr7:151233232-151233873 | Common:1; Rare:116 |