Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:63827057-63827513 | Common:5; Rare:132 | ||||
chr17:64497037-64497136 | Common:1; Rare:41; Clinvar:2; Clinvar (benign):1 | ||||
chr17:64506512-64506785 | Common:3; Rare:99 | ||||
chr17:65056589-65056907 | Common:4; Rare:126 | ||||
chr17:67245166-67245328 | Rare:52 | ||||
chr17:67717750-67717977 | Rare:80 | ||||
chr17:68247849-68248139 | Common:6; Rare:123 | ||||
chr17:68955309-68955499 | Rare:37 | ||||
chr17:69141803-69142036 | Common:2; Rare:50 | ||||
chr17:69502205-69502406 | Rare:37 | ||||
chr17:70169404-70169554 | Rare:40 | ||||
chr17:72120787-72121047 | Rare:69 | ||||
chr17:73232106-73232715 | Common:4; Rare:235 | ||||
chr17:74213334-74213574 | Common:4; Rare:51 | ||||
chr17:74431984-74432107 | Common:1; Rare:58 |