Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150578480-150578779 | Common:1; Rare:86 | ||||
chr1:150579517-150579853 | Common:10; Rare:117 | ||||
chr1:150629119-150629406 | Common:1; Rare:88 | ||||
chr1:150629440-150629792 | Rare:82 | ||||
chr1:150697049-150697474 | Common:1; Rare:90 | ||||
chr1:150926303-150926472 | Rare:48 | ||||
chr1:150974639-150974914 | Common:2; Rare:83 | ||||
chr1:151156492-151156685 | Rare:36 | ||||
chr1:151165858-151166207 | Common:3; Rare:104 | ||||
chr1:151199054-151199112 | Rare:17 | ||||
chr1:151265754-151266038 | Rare:51 | ||||
chr1:151281987-151282337 | Rare:95 | ||||
chr1:151347188-151347350 | Rare:33 | ||||
chr1:151399500-151399610 | Common:2; Rare:44; Clinvar (pathogenic):1 | ||||
chr1:151510110-151510171 | Common:2; Rare:15 |