Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:100607417-100607747 | Rare:94 | ||||
chr7:101223762-101224069 | Common:1; Rare:95 | ||||
chr7:130913195-130913510 | Common:1; Rare:59 | ||||
chr7:135733212-135733234 | Rare:3 | ||||
chr8:37493771-37494040 | Common:3; Rare:44 | ||||
chr8:98147264-98147416 | Common:1; Rare:22 | ||||
chr8:106272432-106272640 | Common:1; Rare:32 | ||||
chr8:127737630-127737797 | Common:1; Rare:48 | ||||
chr8:127794274-127794575 | Rare:76 | ||||
chr8:143816804-143817012 | Common:1; Rare:69 | ||||
chr8:145002892-145003017 | Common:1; Rare:37 | ||||
chr9:6215050-6215159 | Rare:17 | ||||
chr9:14993193-14993371 | Common:2; Rare:65 | ||||
chr9:35684268-35684520 | Rare:56; Clinvar:2; Clinvar (benign):3 | ||||
chr9:37087389-37087547 | Rare:32 |