Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:39409253-39409375 | Rare:23 | ||||
chr1:39409543-39409728 | Rare:39 | ||||
chr1:39491420-39491623 | Common:3; Rare:72 | ||||
chr1:39575266-39575318 | Common:1; Rare:11 | ||||
chr1:39576339-39576527 | Rare:65 | ||||
chr1:39576724-39576963 | Rare:89 | ||||
chr1:39738689-39739028 | Common:3; Rare:90 | ||||
chr1:39739272-39739324 | Rare:8 | ||||
chr1:39788776-39788780 | |||||
chr1:39788803-39789214 | Common:5; Rare:126 | ||||
chr1:39789229-39789298 | Common:1; Rare:14 | ||||
chr1:39883091-39883234 | Rare:24 | ||||
chr1:39883443-39883637 | Common:1; Rare:73; Clinvar (pathogenic):1 | ||||
chr1:39901774-39902116 | Common:6; Rare:109 | ||||
chr1:39954867-39955298 | Common:1; Rare:108 |