Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:47492455-47492753 | Common:2; Rare:99 | ||||
chr17:48071468-48071745 | Rare:46 | ||||
chr17:48996459-48996608 | Common:1; Rare:32 | ||||
chr17:49570016-49570103 | Rare:24 | ||||
chr17:59679101-59679412 | Rare:55 | ||||
chr17:60135674-60135836 | Rare:42 | ||||
chr17:64145753-64145975 | Common:2; Rare:58 | ||||
chr17:64975561-64975708 | Common:1; Rare:49 | ||||
chr17:65100494-65100838 | Common:5; Rare:108 | ||||
chr17:73196655-73196927 | Common:3; Rare:84; Clinvar:3; Clinvar (benign):2 | ||||
chr17:76557614-76557854 | Common:1; Rare:82 | ||||
chr17:76671641-76671966 | Common:3; Rare:81 | ||||
chr17:79949929-79950275 | Rare:64 | ||||
chr18:5238006-5238135 | Common:1; Rare:51 | ||||
chr18:6462519-6462698 | Common:5; Rare:39 |