Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:74062285-74062368 | Rare:16 | ||||
chr7:94397879-94398089 | Rare:26 | ||||
chr7:94410248-94410527 | Rare:61; Clinvar:4; Clinvar (pathogenic):2 | ||||
chr7:100335888-100336151 | Common:1; Rare:85 | ||||
chr7:100607419-100607738 | Rare:90 | ||||
chr7:133034544-133034853 | Common:4; Rare:105 | ||||
chr8:22593628-22593800 | Rare:55 | ||||
chr8:127794372-127794560 | Rare:50 | ||||
chr9:35684247-35684544 | Rare:67; Clinvar:3; Clinvar (benign):4 | ||||
chr9:37087272-37087548 | Common:1; Rare:50 | ||||
chr9:41358594-41358916 | Common:2; Rare:81 | ||||
chr9:87728257-87728808 | Common:2; Rare:143 | ||||
chr9:107734619-107734838 | Common:3; Rare:42 | ||||
chr9:110579022-110579105 | Common:1; Rare:26 | ||||
chr9:124858025-124858133 | Common:1; Rare:37 |