Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:55429088-55429584 | Common:4; Rare:86 | ||||
chr1:55443600-55443847 | Common:3; Rare:41 | ||||
chr1:56578348-56578495 | Rare:35 | ||||
chr1:56578784-56578828 | Rare:17 | ||||
chr1:57674913-57675126 | Rare:42 | ||||
chr1:57796778-57796926 | Rare:28 | ||||
chr1:58545894-58546120 | Common:1; Rare:42 | ||||
chr1:58573839-58574030 | Common:2; Rare:29 | ||||
chr1:58575210-58575269 | Common:1; Rare:9 | ||||
chr1:58575616-58575880 | Common:1; Rare:46; Clinvar:1; Clinvar (benign):2 | ||||
chr1:58576035-58576595 | Common:5; Rare:198; Clinvar:4; Clinvar (benign):5 | ||||
chr1:58576602-58576790 | Common:2; Rare:78; Clinvar (benign):2 | ||||
chr1:58576808-58576975 | Rare:59; Clinvar:1 | ||||
chr1:58576981-58577171 | Rare:61; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr1:58578886-58579017 | Common:5; Rare:22 |