Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:149931528-149931650 | Rare:20 | ||||
chr1:150067150-150067369 | Common:3; Rare:44 | ||||
chr1:150067559-150067899 | Common:1; Rare:92 | ||||
chr1:150234639-150234750 | Rare:22 | ||||
chr1:150268346-150268505 | Rare:34 | ||||
chr1:150268697-150269071 | Common:2; Rare:107 | ||||
chr1:150272388-150272747 | Common:1; Rare:61 | ||||
chr1:150282285-150282596 | Common:3; Rare:63 | ||||
chr1:150293825-150293927 | Common:1; Rare:37 | ||||
chr1:150321390-150321619 | Rare:73; Clinvar:3; Clinvar (benign):1 | ||||
chr1:150364550-150364724 | Common:1; Rare:58 | ||||
chr1:150487301-150487464 | Common:3; Rare:44; Clinvar (benign):3 | ||||
chr1:150578836-150579271 | Common:3; Rare:176 | ||||
chr1:150579574-150579837 | Common:9; Rare:88 | ||||
chr1:150629107-150629305 | Rare:55 |