Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151070444-151070600 | Common:2; Rare:55 | ||||
chr1:151146602-151146857 | Common:1; Rare:61 | ||||
chr1:151156656-151156685 | Rare:5 | ||||
chr1:151165776-151166186 | Common:3; Rare:120 | ||||
chr1:151281947-151282318 | Rare:109 | ||||
chr1:151347233-151347542 | Rare:73 | ||||
chr1:151427932-151428130 | Common:1; Rare:46; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr1:151763457-151763547 | Common:1; Rare:34 | ||||
chr1:151790461-151790851 | Common:2; Rare:86 | ||||
chr1:152036912-152037127 | Common:2; Rare:57 | ||||
chr1:153535328-153535655 | Common:2; Rare:69 | ||||
chr1:153535933-153536305 | Common:3; Rare:72 | ||||
chr1:153544957-153545269 | Common:2; Rare:51 | ||||
chr1:153545759-153545862 | Rare:17 | ||||
chr1:153549238-153549493 | Common:2; Rare:47 |