Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:151165822-151166162 | Common:3; Rare:95 | ||||
chr1:151198362-151198607 | Common:1; Rare:81 | ||||
chr1:151254624-151254785 | Rare:40 | ||||
chr1:151281966-151282318 | Rare:98 | ||||
chr1:151327639-151327768 | Rare:20 | ||||
chr1:151346843-151347037 | Rare:55 | ||||
chr1:151399233-151399605 | Common:8; Rare:89; Clinvar (pathogenic):1 | ||||
chr1:151763326-151763450 | Common:1; Rare:55 | ||||
chr1:151763457-151763554 | Common:1; Rare:34 | ||||
chr1:151790481-151790871 | Common:3; Rare:87 | ||||
chr1:151909375-151909710 | Common:4; Rare:121 | ||||
chr1:151993750-151993985 | Common:4; Rare:83 | ||||
chr1:153535939-153536173 | Common:2; Rare:52 | ||||
chr1:153536219-153536295 | Common:1; Rare:11 | ||||
chr1:153545759-153545870 | Rare:19 |