Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr4:6673898-6674075 | Common:10; Rare:82 | ||||
chr4:82428108-82428343 | Common:2; Rare:73 | ||||
chr4:121669715-121670001 | Common:3; Rare:75 | ||||
chr4:147637322-147637444 | Rare:22 | ||||
chr5:1633941-1634047 | Common:2; Rare:33 | ||||
chr5:8457531-8457723 | Common:1; Rare:69 | ||||
chr5:128083047-128083168 | Common:5; Rare:39 | ||||
chr5:135030227-135030538 | Common:1; Rare:44 | ||||
chr5:137752996-137753221 | Common:1; Rare:77 | ||||
chr5:141319017-141319149 | Rare:24 | ||||
chr5:178209236-178209444 | Rare:83 | ||||
chr5:179833454-179833780 | Common:7; Rare:127; Clinvar:4; Clinvar (benign):6; Clinvar (pathogenic):1 | ||||
chr5:181246433-181246545 | Common:1; Rare:41 | ||||
chr6:21596308-21596498 | Rare:77 | ||||
chr6:34246187-34246522 | Common:1; Rare:80 |