Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:58000628-58000939 | Common:1; Rare:80 | ||||
chr16:58001318-58001526 | Common:1; Rare:74; Clinvar (benign):1 | ||||
chr16:58025439-58025803 | Rare:113 | ||||
chr16:58129252-58129581 | Common:4; Rare:103 | ||||
chr16:58197728-58198020 | Common:1; Rare:76 | ||||
chr16:58198068-58198306 | Rare:85 | ||||
chr16:58515073-58515548 | Common:6; Rare:123 | ||||
chr16:58518529-58518801 | Rare:81 | ||||
chr16:58629763-58630013 | Common:1; Rare:74 | ||||
chr16:58684689-58684820 | Rare:37 | ||||
chr16:58734244-58734397 | Common:4; Rare:49 | ||||
chr16:62036390-62036597 | Rare:54 | ||||
chr16:66549841-66549918 | Rare:23 | ||||
chr16:66552468-66552664 | Rare:84 | ||||
chr16:66604525-66604803 | Rare:72 |