Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr17:80101373-80101625 | Common:4; Rare:112; Clinvar (benign):3 | ||||
chr17:80147115-80147331 | Common:5; Rare:83 | ||||
chr17:80220370-80220453 | Rare:26 | ||||
chr17:80415090-80415189 | Common:1; Rare:64 | ||||
chr17:80991763-80991921 | Common:1; Rare:60 | ||||
chr17:81295273-81295389 | Common:1; Rare:24 | ||||
chr17:81512715-81513117 | Common:7; Rare:213; Clinvar (benign):14 | ||||
chr17:81552322-81552457 | Common:1; Rare:51 | ||||
chr17:81666573-81666763 | Common:1; Rare:81 | ||||
chr17:81683707-81684052 | Common:4; Rare:172 | ||||
chr17:81703277-81703467 | Common:2; Rare:52; Clinvar (benign):1 | ||||
chr17:81833243-81833397 | Rare:68 | ||||
chr17:81871309-81871445 | Rare:47 | ||||
chr17:81891418-81891768 | Common:2; Rare:139 | ||||
chr17:81937257-81937418 | Rare:60 |