Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:17614574-17614646 | Common:2; Rare:34 | ||||
chr4:39458880-39459053 | Common:2; Rare:91 | ||||
chr4:57110075-57110295 | Rare:69 | ||||
chr4:75724419-75724687 | Common:1; Rare:78 | ||||
chr4:83455821-83456078 | Common:2; Rare:100 | ||||
chr4:88523744-88523855 | Common:2; Rare:34 | ||||
chr4:99088696-99088872 | Common:6; Rare:79 | ||||
chr4:99950271-99950527 | Rare:53 | ||||
chr4:102868891-102869024 | Common:1; Rare:39 | ||||
chr4:108620503-108620637 | Common:3; Rare:67 | ||||
chr4:118685319-118685454 | Common:2; Rare:42 | ||||
chr4:121696934-121697099 | Common:4; Rare:48 | ||||
chr4:140373380-140373696 | Common:2; Rare:126 | ||||
chr4:158671982-158672316 | Common:4; Rare:72; Clinvar:2; Clinvar (benign):1 | ||||
chr4:173370696-173370975 | Common:2; Rare:71 |