Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:41990390-41990563 | Common:1; Rare:63 | ||||
chr4:44678640-44678706 | Rare:31 | ||||
chr4:47031512-47031571 | Rare:19 | ||||
chr4:47485211-47485340 | Common:1; Rare:48 | ||||
chr4:48016643-48016784 | Common:1; Rare:42 | ||||
chr4:48341159-48341494 | Common:1; Rare:139 | ||||
chr4:48780247-48780572 | Common:2; Rare:97 | ||||
chr4:55346175-55346332 | Common:3; Rare:51; Clinvar:3; Clinvar (benign):2 | ||||
chr4:55546801-55546996 | Common:2; Rare:69 | ||||
chr4:55547124-55547223 | Common:1; Rare:34 | ||||
chr4:56387435-56387528 | Rare:32 | ||||
chr4:56435475-56436321 | Common:6; Rare:287 | ||||
chr4:56467521-56467655 | Common:1; Rare:51; Clinvar (benign):1 | ||||
chr4:56977597-56977785 | Common:1; Rare:65 | ||||
chr4:65670487-65670565 | Rare:21 |