Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:94404690-94404903 | Rare:50; Clinvar:3 | ||||
chr7:94408304-94408396 | Rare:28; Clinvar:1 | ||||
chr7:94409310-94409608 | Rare:86; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):2 | ||||
chr7:94420385-94420648 | Rare:73; Clinvar:3; Clinvar (benign):5; Clinvar (pathogenic):1 | ||||
chr7:100335862-100336146 | Common:1; Rare:94 | ||||
chr7:105013040-105013169 | Rare:46 | ||||
chr7:107924279-107924577 | Common:2; Rare:52 | ||||
chr7:116211453-116211479 | Rare:9 | ||||
chr7:116211483-116211491 | Rare:2 | ||||
chr7:137721808-137721967 | Rare:25 | ||||
chr7:152436535-152436873 | Rare:115 | ||||
chr8:22221960-22222235 | Rare:55 | ||||
chr8:38770162-38770444 | Common:3; Rare:45 | ||||
chr8:73063070-73063143 | Common:1; Rare:16 | ||||
chr8:98033434-98033657 | Common:3; Rare:51 |