Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:44989432-44989641 | Rare:84 | ||||
chr13:45120406-45120532 | Common:1; Rare:38 | ||||
chr13:45341036-45341644 | Common:4; Rare:271 | ||||
chr13:45418322-45418539 | Rare:64 | ||||
chr13:45464870-45465045 | Rare:53 | ||||
chr13:46052638-46052812 | Common:1; Rare:42 | ||||
chr13:46387203-46387378 | Rare:47 | ||||
chr13:48001221-48001408 | Common:1; Rare:85; Clinvar:3; Clinvar (benign):7 | ||||
chr13:48037692-48037789 | Common:1; Rare:54 | ||||
chr13:48233059-48233475 | Common:3; Rare:144 | ||||
chr13:48303683-48303918 | Rare:72; Clinvar:3; Clinvar (pathogenic):1 | ||||
chr13:48975830-48975932 | Rare:37 | ||||
chr13:48976154-48976246 | Rare:26 | ||||
chr13:48976410-48976666 | Common:3; Rare:91 | ||||
chr13:49247807-49247990 | Rare:53 |