Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:89923171-89923425 | Rare:107 | ||||
chr16:89948559-89948803 | Common:3; Rare:72 | ||||
chr16:89972427-89972635 | Common:1; Rare:82 | ||||
chr16:90019362-90019701 | Common:6; Rare:101 | ||||
chr16:90022520-90022713 | Rare:76 | ||||
chr17:352735-353165 | Common:7; Rare:94 | ||||
chr17:714785-714953 | Common:3; Rare:58 | ||||
chr17:752143-752333 | Common:2; Rare:77 | ||||
chr17:1115351-1115523 | Rare:31 | ||||
chr17:1400048-1400407 | Common:3; Rare:150 | ||||
chr17:1516582-1516978 | Common:2; Rare:141 | ||||
chr17:1684794-1685036 | Common:2; Rare:80; Clinvar:4; Clinvar (benign):1 | ||||
chr17:1716195-1716537 | Common:3; Rare:104 | ||||
chr17:1829805-1830038 | Common:5; Rare:101 | ||||
chr17:2303727-2303987 | Common:2; Rare:97 |