Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:6709265-6709318 | Rare:19 | ||||
chr4:14877551-14877777 | Common:3; Rare:48 | ||||
chr4:38664891-38665018 | Rare:39 | ||||
chr4:53592854-53592953 | Common:2; Rare:21 | ||||
chr4:54727829-54728103 | Common:1; Rare:71; Clinvar:8; Clinvar (benign):12; Clinvar (pathogenic):2 | ||||
chr4:55036549-55036697 | Rare:28 | ||||
chr4:76306583-76306758 | Rare:54 | ||||
chr4:77032163-77032203 | Common:1; Rare:6 | ||||
chr4:77820243-77820377 | Rare:54 | ||||
chr4:84965578-84965654 | Common:1; Rare:23 | ||||
chr4:87482432-87482769 | Common:2; Rare:72 | ||||
chr4:87525693-87525799 | Rare:13 | ||||
chr4:99315896-99316306 | Rare:130 | ||||
chr4:118278505-118278786 | Common:4; Rare:105 | ||||
chr4:118279075-118279192 | Common:3; Rare:32 |