Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr10:122852346-122852587 | Common:1; Rare:40 | ||||
chr15:34795525-34795568 | Common:1; Rare:11; Clinvar:1; Clinvar (benign):2 | ||||
chr15:51094660-51094963 | Common:7; Rare:80 | ||||
chr17:64975577-64975748 | Common:2; Rare:67 | ||||
chr18:5238016-5238125 | Common:1; Rare:47 | ||||
chr22:46069794-46070051 | Rare:58 | ||||
chr3:75435060-75435379 | Common:3; Rare:112 | ||||
chr3:183447433-183447674 | Common:2; Rare:61 | ||||
chr4:76306565-76306758 | Rare:58 | ||||
chr5:150778635-150778833 | Common:2; Rare:80 | ||||
chr5:174825722-174825852 | Rare:26 | ||||
chr6:39819802-39820021 | Common:5; Rare:45 | ||||
chr7:45768945-45769138 | Common:1; Rare:56 | ||||
chr7:66493512-66493737 | Common:4; Rare:95 | ||||
chr7:67302441-67302696 | Common:5; Rare:83 |