Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151165858-151166167 | Common:3; Rare:90 | ||||
chr1:151190129-151190294 | Rare:48 | ||||
chr1:151254435-151254785 | Rare:77 | ||||
chr1:151281941-151282319 | Rare:112 | ||||
chr1:151346834-151347022 | Rare:54 | ||||
chr1:151399494-151399596 | Common:1; Rare:38; Clinvar (pathogenic):1 | ||||
chr1:151790522-151790830 | Common:1; Rare:59 | ||||
chr1:151992617-151992777 | Common:1; Rare:36 | ||||
chr1:151993750-151993994 | Common:4; Rare:88 | ||||
chr1:153535939-153536157 | Common:1; Rare:50 | ||||
chr1:153536227-153536261 | Rare:4 | ||||
chr1:153608916-153609170 | Common:1; Rare:46 | ||||
chr1:153609332-153609480 | Common:2; Rare:23 | ||||
chr1:153633851-153634145 | Common:4; Rare:90 | ||||
chr1:153634317-153634420 | Common:1; Rare:30 |