Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:38667227-38667335 | Rare:16 | ||||
chr4:38816530-38816555 | Rare:5 | ||||
chr4:39472401-39472556 | Rare:21 | ||||
chr4:39976473-39976724 | Rare:84 | ||||
chr4:40563963-40564262 | Common:1; Rare:49 | ||||
chr4:40628695-40628947 | Common:1; Rare:32 | ||||
chr4:54232975-54233145 | Common:4; Rare:40 | ||||
chr4:54233815-54233966 | Rare:33 | ||||
chr4:54267345-54267741 | Common:3; Rare:97; Clinvar:26; Clinvar (benign):15 | ||||
chr4:55397797-55397988 | Common:2; Rare:45 | ||||
chr4:55947916-55948139 | Common:2; Rare:39 | ||||
chr4:57017431-57017728 | Rare:45 | ||||
chr4:57042811-57043029 | Common:1; Rare:47 | ||||
chr4:70689449-70689631 | Rare:44 | ||||
chr4:71186575-71186775 | Common:1; Rare:49 |