Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:42609305-42609720 | Common:8; Rare:175; Clinvar (benign):1 | ||||
chr17:42964441-42964508 | Rare:30 | ||||
chr17:43125481-43125663 | Rare:42; Clinvar (benign):1 | ||||
chr17:43170205-43170412 | Rare:45 | ||||
chr17:43170938-43171235 | Rare:98 | ||||
chr17:43778920-43779276 | Common:3; Rare:85 | ||||
chr17:44123610-44123840 | Common:3; Rare:64 | ||||
chr17:44186720-44187067 | Rare:105 | ||||
chr17:44187152-44187302 | Rare:37 | ||||
chr17:44220852-44221054 | Rare:66 | ||||
chr17:44324774-44325003 | Common:2; Rare:82 | ||||
chr17:44503382-44503717 | Rare:133 | ||||
chr17:44899375-44899477 | Rare:44 | ||||
chr17:45060969-45061416 | Common:2; Rare:135 | ||||
chr17:45316986-45317346 | Common:5; Rare:91 |