Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:5126622-5126756 | Common:2; Rare:34 | ||||
chr20:5610904-5611167 | Common:2; Rare:93 | ||||
chr20:5950467-5950680 | Common:8; Rare:58 | ||||
chr20:13784882-13785053 | Common:2; Rare:70; Clinvar (benign):2 | ||||
chr20:13995246-13995603 | Rare:102 | ||||
chr20:14337561-14337696 | Rare:27 | ||||
chr20:16573313-16573541 | Common:1; Rare:62 | ||||
chr20:17569218-17569437 | Common:3; Rare:43 | ||||
chr20:17569966-17570208 | Common:3; Rare:107 | ||||
chr20:17968422-17968589 | Common:4; Rare:68 | ||||
chr20:17968795-17968935 | Common:1; Rare:60 | ||||
chr20:18467121-18467413 | Rare:61 | ||||
chr20:20017269-20017372 | Rare:42 | ||||
chr20:21303223-21303385 | Rare:62 | ||||
chr20:23350555-23350820 | Common:1; Rare:80 |