Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:38900994-38901314 | Common:2; Rare:75 | ||||
chr8:38996463-38996826 | Common:3; Rare:115 | ||||
chr8:38996907-38997051 | Common:2; Rare:74 | ||||
chr8:42051982-42052272 | Common:1; Rare:84 | ||||
chr8:42391808-42391920 | Common:1; Rare:38 | ||||
chr8:42541128-42541182 | Rare:11 | ||||
chr8:42541554-42541661 | Rare:34 | ||||
chr8:42541691-42542043 | Common:1; Rare:108; Clinvar:3; Clinvar (benign):1 | ||||
chr8:42896596-42897039 | Common:1; Rare:179 | ||||
chr8:47960122-47960191 | Rare:24; Clinvar (benign):1 | ||||
chr8:47960730-47960974 | Common:1; Rare:85; Clinvar:9 | ||||
chr8:51898995-51899326 | Common:6; Rare:148 | ||||
chr8:52714427-52714571 | Common:1; Rare:60 | ||||
chr8:53843223-53843370 | Rare:36 | ||||
chr8:55773346-55773486 | Common:3; Rare:44 |