Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:28100515-28100732 | Common:2; Rare:52 | ||||
chr13:28138107-28138229 | Common:1; Rare:42 | ||||
chr13:28658948-28659040 | Rare:34 | ||||
chr13:28659041-28659194 | Rare:70; Clinvar (pathogenic):1 | ||||
chr13:28718779-28719095 | Common:1; Rare:88 | ||||
chr13:29850121-29850380 | Common:1; Rare:78 | ||||
chr13:30306828-30307207 | Common:6; Rare:105 | ||||
chr13:30307383-30307496 | Common:2; Rare:45 | ||||
chr13:30464090-30464374 | Common:3; Rare:82 | ||||
chr13:30464877-30464984 | Common:1; Rare:34 | ||||
chr13:30465784-30466134 | Common:1; Rare:108 | ||||
chr13:30616980-30617151 | Rare:31 | ||||
chr13:30617290-30618040 | Common:1; Rare:232 | ||||
chr13:30735405-30735671 | Common:2; Rare:68 | ||||
chr13:32031240-32031435 | Common:1; Rare:52 |