Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:16000497-16000866 | Common:2; Rare:89; Clinvar:2; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr4:16055577-16055779 | Rare:45 | ||||
chr4:16256285-16256577 | Common:3; Rare:66 | ||||
chr4:38667213-38667489 | Rare:60 | ||||
chr4:39456423-39456644 | Common:2; Rare:59 | ||||
chr4:40316899-40317169 | Common:2; Rare:43 | ||||
chr4:44680457-44680700 | Rare:62 | ||||
chr4:55947896-55948120 | Common:2; Rare:37 | ||||
chr4:57008668-57008890 | Common:2; Rare:39 | ||||
chr4:74278488-74278527 | Rare:10 | ||||
chr4:74278532-74278643 | Rare:17 | ||||
chr4:77047005-77047183 | Common:1; Rare:30 | ||||
chr4:77820179-77820413 | Rare:95 | ||||
chr4:77854498-77854647 | Rare:16 | ||||
chr4:82894126-82894176 | Rare:8 |