Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:123748898-123749239 | Common:3; Rare:123 | ||||
chr7:124929793-124929933 | Common:3; Rare:47 | ||||
chr7:127585584-127585664 | Rare:26 | ||||
chr7:127588292-127588508 | Rare:92 | ||||
chr7:127651830-127652227 | Common:3; Rare:117 | ||||
chr7:128455729-128455903 | Common:2; Rare:94 | ||||
chr7:128739096-128739432 | Common:3; Rare:97 | ||||
chr7:128830140-128830449 | Common:4; Rare:79 | ||||
chr7:128830549-128830760 | Rare:71; Clinvar:5; Clinvar (benign):3 | ||||
chr7:128910677-128910841 | Common:2; Rare:48 | ||||
chr7:129054836-129055239 | Common:2; Rare:82 | ||||
chr7:129611616-129611798 | Common:1; Rare:58 | ||||
chr7:130070295-130070572 | Common:1; Rare:74 | ||||
chr7:130205372-130205574 | Rare:90 | ||||
chr7:130440981-130441337 | Common:3; Rare:150; Clinvar:2; Clinvar (benign):2 |