Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr7:139109328-139109498 | Common:1; Rare:51 | ||||
chr7:139133675-139133828 | Rare:40 | ||||
chr7:139341166-139341369 | Rare:46 | ||||
chr7:141551311-141551423 | Rare:36; Clinvar:4; Clinvar (benign):2 | ||||
chr7:141738033-141738457 | Common:4; Rare:132 | ||||
chr7:142855000-142855167 | Common:3; Rare:49 | ||||
chr7:143902107-143902276 | Common:5; Rare:57 | ||||
chr7:149126209-149126428 | Common:6; Rare:74 | ||||
chr7:151028155-151028471 | Rare:105 | ||||
chr7:151080793-151080973 | Rare:59 | ||||
chr7:151232396-151232528 | Rare:42 | ||||
chr7:152025567-152025767 | Rare:80 | ||||
chr7:155644384-155644719 | Common:2; Rare:112 | ||||
chr7:156640556-156640791 | Common:2; Rare:111 | ||||
chr7:157336776-157337066 | Common:2; Rare:138; Clinvar:1 |