Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:66691689-66691979 | Common:3; Rare:54 | ||||
chr17:66697764-66697887 | Common:2; Rare:19 | ||||
chr17:66698234-66698446 | Common:1; Rare:34 | ||||
chr17:66701275-66701366 | Common:1; Rare:11 | ||||
chr17:67347279-67347353 | Rare:18 | ||||
chr17:67954007-67954321 | Common:7; Rare:60 | ||||
chr17:68040650-68040890 | Common:3; Rare:64 | ||||
chr17:68043791-68043861 | Rare:32 | ||||
chr17:72422903-72423057 | Rare:33 | ||||
chr17:72427514-72427561 | Rare:11 | ||||
chr17:72428231-72428471 | Rare:34 | ||||
chr17:73191636-73191712 | Common:3; Rare:18 | ||||
chr17:74768117-74768577 | Common:1; Rare:165 | ||||
chr17:74862584-74863193 | Common:6; Rare:186; Clinvar:2; Clinvar (pathogenic):2 | ||||
chr17:74982306-74982399 | Common:1; Rare:27 |