Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:68511806-68512039 | Rare:56 | ||||
chr17:69327091-69327334 | Common:2; Rare:81 | ||||
chr17:73232210-73232711 | Common:3; Rare:185 | ||||
chr17:74776295-74776540 | Common:4; Rare:79 | ||||
chr17:75012482-75012689 | Common:1; Rare:42 | ||||
chr17:75182874-75183291 | Common:1; Rare:132 | ||||
chr17:75205421-75205734 | Rare:91 | ||||
chr17:75261598-75261925 | Common:4; Rare:97; Clinvar (benign):1 | ||||
chr17:75639946-75640122 | Common:1; Rare:40 | ||||
chr17:75667173-75667370 | Common:4; Rare:60 | ||||
chr17:75979103-75979283 | Rare:50; Clinvar:4 | ||||
chr17:76103719-76103864 | Common:4; Rare:44 | ||||
chr17:76726464-76726865 | Common:5; Rare:144 | ||||
chr17:76737328-76737537 | Common:2; Rare:79 | ||||
chr17:78187045-78187365 | Common:3; Rare:101 |