Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:133051862-133052107 | Rare:92 | ||||
chr5:133968587-133968791 | Common:1; Rare:75 | ||||
chr5:134004654-134004834 | Common:1; Rare:68 | ||||
chr5:134411826-134412008 | Rare:69 | ||||
chr5:134648726-134648816 | Rare:20 | ||||
chr5:134845865-134846057 | Rare:87 | ||||
chr5:134874236-134874400 | Common:1; Rare:77 | ||||
chr5:135399138-135399369 | Rare:61 | ||||
chr5:138338203-138338267 | Common:1; Rare:28 | ||||
chr5:138543095-138543496 | Common:2; Rare:118 | ||||
chr5:139198284-139198531 | Rare:83; Clinvar (benign):1 | ||||
chr5:139561721-139561792 | Rare:34 | ||||
chr5:140303057-140303191 | Common:1; Rare:43 | ||||
chr5:140346597-140346721 | Common:1; Rare:34 | ||||
chr5:140647603-140647873 | Common:5; Rare:110; Clinvar:4; Clinvar (benign):3 |