Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:43171043-43171255 | Rare:67 | ||||
chr17:43778922-43779098 | Common:1; Rare:45 | ||||
chr17:44111225-44111438 | Rare:60 | ||||
chr17:44186672-44186998 | Common:1; Rare:116 | ||||
chr17:44187150-44187274 | Rare:32 | ||||
chr17:44220819-44221025 | Rare:64 | ||||
chr17:44221269-44221353 | Rare:27 | ||||
chr17:44324765-44324989 | Common:2; Rare:82 | ||||
chr17:44899375-44899736 | Common:2; Rare:112; Clinvar:1; Clinvar (benign):1 | ||||
chr17:45060993-45061341 | Common:2; Rare:93 | ||||
chr17:45132288-45132631 | Common:2; Rare:105 | ||||
chr17:45148170-45148615 | Common:1; Rare:158 | ||||
chr17:45161530-45161864 | Common:1; Rare:73 | ||||
chr17:45431912-45432214 | Common:2; Rare:40 | ||||
chr17:46193497-46193600 | Common:1; Rare:32 |