Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:56451320-56451562 | Not yet | Common:1; Rare:64 | 288 | ||
chr16:57447359-57447491 | Not yet | Common:2; Rare:35; Clinvar:2; Clinvar (benign):1 | 148 | ||
chr16:70523538-70523834 | Not yet | Common:3; Rare:92 | 377 | ||
chr16:75647647-75647824 | Not yet | Common:2; Rare:79; Clinvar:2 | 308 | ||
chr16:85799509-85799702 | Not yet | Common:2; Rare:56 | 177 | ||
chr17:28335451-28335781 | Not yet | Common:1; Rare:75 | 342 | ||
chr17:28357509-28357658 | Not yet | Rare:70 | 205 | ||
chr17:42609362-42609664 | Not yet | Common:5; Rare:112 | 349 | ||
chr17:45061107-45061339 | Not yet | Common:1; Rare:65 | 243 | ||
chr17:47831516-47831623 | Not yet | Rare:28 | 158 | ||
chr17:59707402-59707665 | Not yet | Common:3; Rare:74; Clinvar (benign):2 | 334 | ||
chr17:75046943-75047194 | Not yet | Common:1; Rare:75 | 289 | ||
chr17:75261604-75261930 | Not yet | Common:4; Rare:97; Clinvar (benign):2 | 292 | ||
chr17:75979126-75979272 | Not yet | Rare:38; Clinvar:4 | 164 | ||
chr17:81703292-81703496 | Not yet | Common:2; Rare:57; Clinvar (benign):2 | 247 |