Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:150629534-150629859 | Common:1; Rare:72 | ||||
chr1:150697177-150697474 | Common:1; Rare:63 | ||||
chr1:150926213-150926452 | Rare:71 | ||||
chr1:151165851-151166162 | Common:3; Rare:87 | ||||
chr1:151198384-151198609 | Common:1; Rare:78 | ||||
chr1:151254624-151254785 | Rare:40 | ||||
chr1:151281946-151282327 | Rare:112 | ||||
chr1:151346834-151347042 | Rare:57 | ||||
chr1:151347233-151347499 | Rare:64 | ||||
chr1:151399432-151399602 | Common:1; Rare:55; Clinvar (pathogenic):1 | ||||
chr1:151511150-151511403 | Common:3; Rare:57 | ||||
chr1:151540137-151540319 | Rare:51 | ||||
chr1:151763434-151763609 | Common:3; Rare:74 | ||||
chr1:151790452-151790863 | Common:3; Rare:97 | ||||
chr1:151909392-151909714 | Common:4; Rare:115 |