Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr13:28659071-28659194 | Rare:52; Clinvar (pathogenic):1 | ||||
chr13:28718787-28718948 | Rare:46 | ||||
chr13:28718950-28719123 | Common:1; Rare:37 | ||||
chr13:30306805-30307207 | Common:7; Rare:112 | ||||
chr13:30307377-30307596 | Common:2; Rare:76 | ||||
chr13:30464208-30464372 | Common:1; Rare:49 | ||||
chr13:30616981-30617146 | Rare:31 | ||||
chr13:30617242-30617383 | Rare:28 | ||||
chr13:30617479-30618056 | Common:1; Rare:186 | ||||
chr13:30735395-30735608 | Common:2; Rare:46 | ||||
chr13:30906649-30906793 | Common:1; Rare:45 | ||||
chr13:32031507-32031605 | Rare:19 | ||||
chr13:32031611-32031790 | Common:1; Rare:55 | ||||
chr13:32254094-32254389 | Common:3; Rare:68 | ||||
chr13:32315422-32315529 | Rare:30; Clinvar:1 |