Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:39458864-39459075 | Common:3; Rare:115; Clinvar (benign):1 | ||||
chr4:39527405-39527754 | Common:2; Rare:85 | ||||
chr4:39527959-39528021 | Rare:13 | ||||
chr4:39638847-39639149 | Common:1; Rare:112 | ||||
chr4:39697931-39698227 | Common:2; Rare:126 | ||||
chr4:39977310-39977651 | Common:2; Rare:101 | ||||
chr4:40056862-40056930 | Rare:20 | ||||
chr4:40630835-40630929 | Rare:25 | ||||
chr4:41360668-41360843 | Common:1; Rare:47 | ||||
chr4:41990401-41990578 | Common:1; Rare:64 | ||||
chr4:42656919-42657304 | Common:7; Rare:130 | ||||
chr4:44678364-44678496 | Rare:44 | ||||
chr4:44678624-44678706 | Rare:38 | ||||
chr4:44726475-44726631 | Common:2; Rare:55 | ||||
chr4:47485198-47485340 | Common:1; Rare:53 |