Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151265716-151266103 | Common:2; Rare:80 | ||||
chr1:151281923-151282323 | Rare:116 | ||||
chr1:151327641-151327856 | Common:2; Rare:44 | ||||
chr1:151347233-151347499 | Rare:64 | ||||
chr1:151399344-151399640 | Common:3; Rare:90; Clinvar (pathogenic):2 | ||||
chr1:151511150-151511464 | Common:4; Rare:65 | ||||
chr1:151763457-151763522 | Common:1; Rare:23 | ||||
chr1:151790461-151790830 | Common:2; Rare:82 | ||||
chr1:151909397-151909569 | Common:1; Rare:68 | ||||
chr1:151993756-151993985 | Common:4; Rare:81 | ||||
chr1:152325236-152325446 | Common:1; Rare:35 | ||||
chr1:153535933-153536299 | Common:3; Rare:72 | ||||
chr1:153545795-153545886 | Rare:17 | ||||
chr1:153612970-153613273 | Common:1; Rare:57 | ||||
chr1:153616304-153616578 | Common:1; Rare:51 |