Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:32927870-32928235 | Common:2; Rare:122 | ||||
chr17:34255155-34255321 | Rare:46 | ||||
chr17:34961396-34961607 | Common:1; Rare:104 | ||||
chr17:34980381-34980607 | Common:4; Rare:66 | ||||
chr17:35119814-35119877 | Rare:30; Clinvar:1; Clinvar (benign):1 | ||||
chr17:35242891-35243087 | Rare:65 | ||||
chr17:35578476-35578726 | Common:1; Rare:64; Clinvar:1; Clinvar (benign):1 | ||||
chr17:35587160-35587635 | Rare:119 | ||||
chr17:35809268-35809572 | Rare:129 | ||||
chr17:36486471-36486724 | Common:3; Rare:89 | ||||
chr17:36534803-36535016 | Common:3; Rare:90 | ||||
chr17:36544772-36545097 | Common:6; Rare:95 | ||||
chr17:36545322-36545709 | Common:2; Rare:140 | ||||
chr17:37359223-37359531 | Common:1; Rare:84 | ||||
chr17:37406749-37406935 | Rare:76 |