Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:24512705-24512860 | Common:3; Rare:41 | ||||
chr13:24922773-24923121 | Common:2; Rare:118; Clinvar:1 | ||||
chr13:26221787-26221995 | Rare:61 | ||||
chr13:26222243-26222362 | Common:2; Rare:34 | ||||
chr13:27251227-27251632 | Common:8; Rare:127 | ||||
chr13:27270696-27270837 | Rare:47 | ||||
chr13:27450119-27450230 | Common:3; Rare:33 | ||||
chr13:27450518-27450685 | Common:2; Rare:64 | ||||
chr13:27620440-27620836 | Common:3; Rare:133 | ||||
chr13:27621074-27621191 | Common:1; Rare:29 | ||||
chr13:27967262-27967527 | Common:2; Rare:58 | ||||
chr13:28138117-28138229 | Common:1; Rare:38 | ||||
chr13:28138632-28138910 | Common:1; Rare:64 | ||||
chr13:28658948-28659009 | Rare:15 | ||||
chr13:28659066-28659181 | Rare:50; Clinvar (pathogenic):1 |