Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:17569218-17569241 | Rare:5 | ||||
chr20:17569966-17570210 | Common:3; Rare:108 | ||||
chr20:17968421-17968653 | Common:4; Rare:103 | ||||
chr20:17968770-17969111 | Common:4; Rare:125 | ||||
chr20:18466989-18467448 | Common:1; Rare:102 | ||||
chr20:18507425-18507619 | Rare:52; Clinvar:1 | ||||
chr20:18507663-18507961 | Common:2; Rare:84; Clinvar:5; Clinvar (benign):2 | ||||
chr20:18567339-18567543 | Common:1; Rare:74 | ||||
chr20:19889289-19889574 | Common:2; Rare:57 | ||||
chr20:20017251-20017399 | Rare:53 | ||||
chr20:20038421-20038669 | Common:1; Rare:48 | ||||
chr20:21303247-21303410 | Rare:62 | ||||
chr20:23049665-23049786 | Common:3; Rare:39 | ||||
chr20:23086355-23086498 | Rare:31 | ||||
chr20:23350489-23350830 | Common:4; Rare:102 |