Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:38402839-38403241 | Common:18; Rare:152 | ||||
chr10:43362259-43362447 | Common:3; Rare:40 | ||||
chr10:43420560-43420670 | Common:4; Rare:35 | ||||
chr10:43690168-43690332 | Rare:41 | ||||
chr10:45001042-45001197 | Common:2; Rare:51 | ||||
chr10:46786614-46786753 | Rare:19 | ||||
chr10:46786774-46786895 | Rare:8 | ||||
chr10:47553472-47553629 | Rare:18 | ||||
chr10:48448906-48449049 | Rare:19 | ||||
chr10:49113819-49113914 | Common:1; Rare:20 | ||||
chr10:49987256-49987383 | Common:1; Rare:28 | ||||
chr10:50622919-50623177 | Common:2; Rare:72 | ||||
chr10:50623207-50623466 | Common:1; Rare:62 | ||||
chr10:51467814-51468062 | Rare:63; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr10:53029912-53030116 | Rare:47 |