Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:143931996-143932189 | Common:2; Rare:111; Clinvar:6; Clinvar (benign):5 | ||||
chr8:144316857-144317027 | Rare:68; Clinvar (pathogenic):1 | ||||
chr8:144393533-144393677 | Common:1; Rare:77 | ||||
chr8:145002835-145003045 | Common:2; Rare:73 | ||||
chr9:686454-686829 | Common:4; Rare:92 | ||||
chr9:4510956-4511215 | Rare:57 | ||||
chr9:4665336-4665594 | Rare:57 | ||||
chr9:5629725-5629936 | Rare:51 | ||||
chr9:6716074-6716198 | Rare:43 | ||||
chr9:6716404-6716567 | Common:2; Rare:54 | ||||
chr9:12784454-12784742 | Common:3; Rare:67 | ||||
chr9:15489984-15490340 | Common:1; Rare:90 | ||||
chr9:19050203-19050501 | Rare:58 | ||||
chr9:19124465-19124759 | Common:2; Rare:45 | ||||
chr9:19126395-19126734 | Common:2; Rare:89 |