Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr6:134633294-134633461 | Common:1; Rare:42 | ||||
chr6:135183078-135183224 | Rare:32 | ||||
chr6:135498418-135498430 | Rare:2 | ||||
chr6:136791498-136791549 | Rare:12 | ||||
chr6:137866321-137866383 | Common:1; Rare:10 | ||||
chr6:137868193-137868252 | Rare:8 | ||||
chr6:140663874-140664016 | Common:1; Rare:22 | ||||
chr6:142945722-142945858 | Rare:30 | ||||
chr6:142946261-142946604 | Common:3; Rare:84 | ||||
chr6:144286211-144286539 | Common:4; Rare:68 | ||||
chr6:150857020-150857060 | Common:1; Rare:8 | ||||
chr6:151291518-151291539 | Rare:7 | ||||
chr6:151494675-151494853 | Common:2; Rare:42 | ||||
chr6:151763503-151763620 | Common:3; Rare:20 | ||||
chr6:152132150-152132377 | Common:2; Rare:51; Clinvar:2; Clinvar (benign):2 |