Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:46052679-46052848 | Common:2; Rare:46 | ||||
chr13:46182114-46182414 | Common:3; Rare:52 | ||||
chr13:46387143-46387367 | Common:1; Rare:56 | ||||
chr13:46387409-46387579 | Common:1; Rare:36 | ||||
chr13:48233382-48233468 | Common:2; Rare:34 | ||||
chr13:48303657-48304049 | Common:1; Rare:128; Clinvar:15; Clinvar (benign):7; Clinvar (pathogenic):2 | ||||
chr13:49247807-49247982 | Rare:50 | ||||
chr13:49443997-49444493 | Common:1; Rare:157 | ||||
chr13:49445199-49445381 | Common:1; Rare:35 | ||||
chr13:49495861-49496077 | Rare:54 | ||||
chr13:49628376-49628547 | Common:1; Rare:38 | ||||
chr13:50081960-50082307 | Common:1; Rare:98 | ||||
chr13:50909901-50910423 | Common:2; Rare:136; Clinvar:3 | ||||
chr13:51453021-51453415 | Common:1; Rare:150 | ||||
chr13:51584762-51584864 | Rare:37 |