Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:24512709-24512842 | Common:3; Rare:37 | ||||
chr13:24922803-24923030 | Common:1; Rare:69; Clinvar:1 | ||||
chr13:26221787-26221932 | Rare:36 | ||||
chr13:26222246-26222386 | Common:2; Rare:41 | ||||
chr13:27251235-27251605 | Common:7; Rare:113 | ||||
chr13:27450130-27450228 | Common:3; Rare:29 | ||||
chr13:27450529-27450651 | Common:2; Rare:48 | ||||
chr13:27620480-27620821 | Common:2; Rare:110 | ||||
chr13:28138119-28138224 | Common:1; Rare:34 | ||||
chr13:28659042-28659180 | Rare:64; Clinvar (pathogenic):1 | ||||
chr13:28718823-28718880 | Rare:15 | ||||
chr13:30306832-30307197 | Common:6; Rare:98 | ||||
chr13:30307390-30307574 | Common:2; Rare:67 | ||||
chr13:30464877-30464978 | Common:1; Rare:34 | ||||
chr13:30617290-30618034 | Common:1; Rare:229 |