Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr22:35894911-35895139 | Common:1; Rare:57 | ||||
chr22:36288725-36289297 | Common:2; Rare:173; Clinvar:6; Clinvar (benign):10 | ||||
chr22:36293826-36294187 | Common:5; Rare:107; Clinvar:1; Clinvar (benign):5 | ||||
chr22:36329721-36329763 | Rare:8 | ||||
chr22:36330680-36330968 | Common:1; Rare:49 | ||||
chr22:36331568-36331729 | Common:2; Rare:28 | ||||
chr22:36471073-36471218 | Common:1; Rare:26 | ||||
chr22:37807059-37807132 | Rare:20 | ||||
chr22:38740999-38741122 | Rare:30 | ||||
chr22:38954033-38954144 | Common:1; Rare:19 | ||||
chr22:41393687-41393958 | Common:5; Rare:62 | ||||
chr22:41413872-41414075 | Common:1; Rare:63 | ||||
chr22:41522686-41522951 | Rare:54; Clinvar (pathogenic):1 | ||||
chr22:41523058-41523278 | Rare:55 | ||||
chr22:42937530-42937712 | Rare:31 |