Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:124539042-124539189 | Common:2; Rare:82; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr8:124998196-124998541 | Common:1; Rare:134 | ||||
chr8:125091731-125091877 | Common:1; Rare:49; Clinvar (benign):2 | ||||
chr8:127735890-127736081 | Rare:44 | ||||
chr8:141001192-141001428 | Common:2; Rare:82 | ||||
chr8:143018408-143018545 | Rare:37 | ||||
chr8:143334851-143334987 | Common:1; Rare:41 | ||||
chr8:143558267-143558381 | Common:1; Rare:43 | ||||
chr8:143829310-143829475 | Rare:60 | ||||
chr8:143939540-143939841 | Common:5; Rare:82 | ||||
chr8:144082517-144082670 | Common:2; Rare:54 | ||||
chr8:144413548-144413719 | Rare:51; Clinvar:1 | ||||
chr8:144853050-144853303 | Common:2; Rare:71 | ||||
chr9:2844047-2844320 | Common:5; Rare:102 | ||||
chr9:4679437-4679657 | Rare:106 |