Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151511234-151511514 | Common:4; Rare:66 | ||||
chr1:151612141-151612380 | Common:1; Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr1:151763443-151763516 | Rare:30 | ||||
chr1:151790436-151790856 | Common:2; Rare:99 | ||||
chr1:151831725-151831852 | Common:1; Rare:36; Clinvar:1; Clinvar (benign):1 | ||||
chr1:151909837-151909929 | Common:1; Rare:25 | ||||
chr1:151993752-151993994 | Common:4; Rare:88 | ||||
chr1:153535923-153536157 | Common:1; Rare:54 | ||||
chr1:153536211-153536287 | Rare:13 | ||||
chr1:153608916-153609032 | Common:1; Rare:18 | ||||
chr1:153612957-153613283 | Common:1; Rare:63 | ||||
chr1:153616293-153616445 | Common:1; Rare:27 | ||||
chr1:153634353-153634434 | Common:1; Rare:26 | ||||
chr1:153670926-153671247 | Rare:109 | ||||
chr1:153678618-153678655 | Rare:8 |