Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:50667545-50667570 | Rare:12 | ||||
chr5:51383261-51383460 | Common:2; Rare:76 | ||||
chr5:52787813-52787957 | Common:1; Rare:27 | ||||
chr5:53109725-53109870 | Common:1; Rare:76; Clinvar:2 | ||||
chr5:54310507-54310711 | Rare:65 | ||||
chr5:55307650-55308028 | Common:4; Rare:128 | ||||
chr5:55994815-55995146 | Rare:113 | ||||
chr5:56952103-56952325 | Rare:85 | ||||
chr5:57173538-57173888 | Common:3; Rare:131 | ||||
chr5:58460076-58460192 | Common:3; Rare:47 | ||||
chr5:59768517-59768761 | Rare:60 | ||||
chr5:60488050-60488291 | Rare:44 | ||||
chr5:60700098-60700233 | Common:1; Rare:51 | ||||
chr5:60945038-60945245 | Common:4; Rare:78; Clinvar:2; Clinvar (benign):4 | ||||
chr5:61162359-61162558 | Common:1; Rare:53 |