Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:50345929-50346146 | Common:4; Rare:72 | ||||
chr17:50373160-50373265 | Common:3; Rare:44 | ||||
chr17:50719463-50719652 | Rare:73 | ||||
chr17:51166274-51166497 | Common:1; Rare:48 | ||||
chr17:51166719-51166854 | Rare:46 | ||||
chr17:51260352-51260601 | Common:3; Rare:115 | ||||
chr17:54968619-54968792 | Common:3; Rare:84 | ||||
chr17:56914022-56914186 | Rare:43 | ||||
chr17:57084980-57085131 | Rare:55 | ||||
chr17:57849998-57850274 | Common:1; Rare:91 | ||||
chr17:57988175-57988541 | Common:5; Rare:107 | ||||
chr17:58219212-58219372 | Common:1; Rare:63; Clinvar:2; Clinvar (benign):4 | ||||
chr17:58692520-58692650 | Common:2; Rare:70; Clinvar:5; Clinvar (benign):16 | ||||
chr17:59106727-59107134 | Common:2; Rare:132; Clinvar:4; Clinvar (benign):2 | ||||
chr17:59155141-59155440 | Common:2; Rare:75 |