Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:135147891-135148109 | Common:1; Rare:45 | ||||
chr7:135170651-135170826 | Common:2; Rare:68 | ||||
chr7:139359672-139360024 | Common:3; Rare:133 | ||||
chr7:141551342-141551423 | Rare:23; Clinvar:4; Clinvar (benign):2 | ||||
chr7:141738033-141738464 | Common:4; Rare:132 | ||||
chr7:142854989-142855264 | Common:6; Rare:66 | ||||
chr7:143288165-143288360 | Rare:62 | ||||
chr7:144195594-144195858 | Rare:4 | ||||
chr7:144355178-144355493 | Rare:2 | ||||
chr7:148698567-148698962 | Common:3; Rare:141 | ||||
chr7:149090656-149090876 | Rare:65 | ||||
chr7:149126234-149126449 | Common:6; Rare:73 | ||||
chr7:151024468-151024617 | Common:1; Rare:24 | ||||
chr7:151028280-151028507 | Rare:102 | ||||
chr7:151057887-151058205 | Common:3; Rare:81 |