Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:143816781-143817012 | Common:1; Rare:74 | ||||
chr8:143932011-143932189 | Common:2; Rare:103; Clinvar:6; Clinvar (benign):5 | ||||
chr8:143937414-143937563 | Rare:42 | ||||
chr8:144313599-144313909 | Common:10; Rare:131 | ||||
chr8:145002825-145003008 | Common:2; Rare:60 | ||||
chr9:693667-693754 | Rare:20 | ||||
chr9:15468961-15469203 | Common:2; Rare:74 | ||||
chr9:16337447-16337662 | Rare:48 | ||||
chr9:35491914-35492071 | Common:1; Rare:20 | ||||
chr9:35723954-35724227 | Rare:67 | ||||
chr9:35909324-35909499 | Common:3; Rare:45 | ||||
chr9:38074398-38074591 | Common:3; Rare:31 | ||||
chr9:40746885-40747184 | Common:1; Rare:73 | ||||
chr9:40992021-40992356 | Common:7; Rare:27 | ||||
chr9:62802025-62802066 | Rare:1 |