Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:36605541-36605816 | Common:2; Rare:101 | ||||
chr20:37178865-37179205 | Rare:101 | ||||
chr20:37527800-37528196 | Common:5; Rare:141 | ||||
chr20:38033415-38033914 | Common:3; Rare:140 | ||||
chr20:44210696-44211117 | Common:5; Rare:153 | ||||
chr20:44475780-44475954 | Common:1; Rare:72 | ||||
chr20:44966370-44966560 | Rare:76 | ||||
chr20:45362948-45363257 | Rare:98 | ||||
chr20:45363357-45363513 | Common:1; Rare:36 | ||||
chr20:45406537-45406736 | Rare:53 | ||||
chr20:45791907-45792014 | Common:1; Rare:42 | ||||
chr20:45827244-45827595 | Common:2; Rare:60 | ||||
chr20:45833250-45833433 | Common:1; Rare:26 | ||||
chr20:45857314-45857630 | Common:3; Rare:88 | ||||
chr20:45891010-45891387 | Common:3; Rare:115; Clinvar:8; Clinvar (benign):3 |