Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:155255166-155256100 | Common:8; Rare:226 | ||||
chr1:155261841-155262042 | Rare:85 | ||||
chr1:155262099-155262526 | Common:5; Rare:248 | ||||
chr1:155273175-155273639 | Rare:188 | ||||
chr1:155277184-155277526 | Rare:155 | ||||
chr1:155308576-155309019 | Common:2; Rare:185 | ||||
chr1:155323796-155323940 | Rare:55 | ||||
chr1:155324000-155324593 | Common:6; Rare:311 | ||||
chr1:155562490-155562700 | Common:1; Rare:110 | ||||
chr1:155562615-155562992 | Common:2; Rare:331 | ||||
chr1:155563076-155563457 | Common:1; Rare:205 | ||||
chr1:155609959-155610304 | Common:9; Rare:188; Clinvar (pathogenic):1 | ||||
chr1:155688417-155688862 | Common:4; Rare:182 | ||||
chr1:155857161-155857366 | Rare:53 | ||||
chr1:155859270-155859660 | Common:5; Rare:141 |