Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:26857513-26857732 | Common:4; Rare:67 | ||||
chr4:26860586-26860849 | Common:3; Rare:91 | ||||
chr4:37826579-37826729 | Common:1; Rare:55 | ||||
chr4:39458843-39459103 | Common:3; Rare:147; Clinvar (benign):4 | ||||
chr4:39527367-39527742 | Common:2; Rare:90 | ||||
chr4:41261741-41261921 | Rare:69; Clinvar:1 | ||||
chr4:44678615-44678778 | Rare:72 | ||||
chr4:48016645-48016784 | Common:1; Rare:42 | ||||
chr4:48269843-48269996 | Common:1; Rare:25 | ||||
chr4:52659199-52659539 | Common:1; Rare:107 | ||||
chr4:56387428-56387518 | Rare:32 | ||||
chr4:56435554-56435797 | Common:3; Rare:75 | ||||
chr4:56436118-56436523 | Rare:139 | ||||
chr4:56467532-56467674 | Common:2; Rare:63; Clinvar (benign):4 | ||||
chr4:57109894-57109968 | Rare:19 |