Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:12811529-12811606 | Common:1; Rare:21 | ||||
chr8:29748117-29748496 | Common:2; Rare:64 | ||||
chr8:143816657-143816941 | Common:1; Rare:89 | ||||
chr9:12710476-12710816 | Common:3; Rare:102 | ||||
chr9:20684756-20684836 | Rare:12 | ||||
chr9:26928109-26928393 | Rare:78 | ||||
chr9:40992070-40992320 | Common:7; Rare:19 | ||||
chr9:62802665-62802780 | |||||
chr9:83219218-83219357 | Common:2; Rare:36 | ||||
chr9:87728088-87728750 | Common:2; Rare:176 | ||||
chr9:87730962-87731066 | Rare:28 | ||||
chr9:100303825-100304095 | Rare:55 | ||||
chr9:103204990-103205253 | Common:7; Rare:57 | ||||
chr9:124353579-124353802 | Rare:55 | ||||
chr9:127868063-127868357 | Common:5; Rare:74; Clinvar (benign):1; Clinvar (pathogenic):1 |