Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:28812402-28812671 | Common:1; Rare:70 | ||||
chr17:28842755-28842863 | Rare:39 | ||||
chr17:28854984-28855032 | Rare:15 | ||||
chr17:28897607-28897761 | Common:1; Rare:50 | ||||
chr17:29140379-29140508 | Common:3; Rare:42 | ||||
chr17:29294064-29294338 | Common:3; Rare:122 | ||||
chr17:29568514-29568740 | Common:2; Rare:72 | ||||
chr17:30477274-30477429 | Rare:40 | ||||
chr17:30824581-30824835 | Common:3; Rare:102 | ||||
chr17:30906210-30906336 | Common:1; Rare:33 | ||||
chr17:32142312-32142589 | Common:6; Rare:129 | ||||
chr17:32350026-32350217 | Rare:103 | ||||
chr17:32444202-32444513 | Common:2; Rare:102 | ||||
chr17:34961402-34961561 | Rare:74 | ||||
chr17:35578539-35578704 | Common:1; Rare:42; Clinvar (benign):1 |