Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr1:8359918-8360160 | Rare:80; Clinvar (benign):1 | ||||
chr1:9038496-9038799 | Common:1; Rare:77 | ||||
chr1:9038990-9039279 | Common:1; Rare:45 | ||||
chr1:9295980-9296233 | Common:1; Rare:47 | ||||
chr1:9303181-9303266 | Rare:6 | ||||
chr1:9730759-9730806 | Rare:11 | ||||
chr1:9731774-9731994 | Common:1; Rare:70 | ||||
chr1:10475709-10475882 | Common:3; Rare:37 | ||||
chr1:10654417-10654732 | Rare:83 | ||||
chr1:10665620-10665871 | Common:2; Rare:37 | ||||
chr1:10683320-10683512 | Common:1; Rare:42 | ||||
chr1:11070952-11071214 | Rare:60 | ||||
chr1:12618294-12618423 | Rare:21 | ||||
chr1:13892961-13893227 | Common:2; Rare:73 | ||||
chr1:15158077-15158179 | Common:3; Rare:15 |