Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:16573297-16573547 | Common:1; Rare:72 | ||||
chr20:17569949-17570230 | Common:3; Rare:119 | ||||
chr20:17968391-17968590 | Common:5; Rare:80 | ||||
chr20:17968784-17969127 | Common:3; Rare:121 | ||||
chr20:18467023-18467132 | Rare:27 | ||||
chr20:18467136-18467460 | Common:2; Rare:69 | ||||
chr20:19889289-19889546 | Common:2; Rare:46 | ||||
chr20:20017231-20017372 | Rare:52 | ||||
chr20:21303244-21303462 | Rare:72 | ||||
chr20:23049653-23049798 | Common:3; Rare:45; Clinvar (pathogenic):1 | ||||
chr20:23086310-23086467 | Rare:28 | ||||
chr20:23350484-23350840 | Common:4; Rare:108 | ||||
chr20:23361807-23361997 | Common:3; Rare:67 | ||||
chr20:24992680-24992833 | Common:4; Rare:70 | ||||
chr20:25290300-25290612 | Common:3; Rare:113 |