Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:62387002-62387133 | Common:3; Rare:55 | ||||
chr20:62937893-62938165 | Common:1; Rare:96 | ||||
chr20:62952591-62952757 | Common:2; Rare:43 | ||||
chr20:63520417-63520883 | Common:8; Rare:188 | ||||
chr20:63707275-63707449 | Rare:55 | ||||
chr20:63707854-63708126 | Rare:80 | ||||
chr20:63865065-63865346 | Common:2; Rare:105 | ||||
chr20:63895120-63895217 | Common:1; Rare:46; Clinvar:4; Clinvar (benign):2 | ||||
chr20:63956378-63956705 | Common:1; Rare:125 | ||||
chr21:25734840-25735427 | Common:3; Rare:207 | ||||
chr21:25735595-25735828 | Common:3; Rare:57 | ||||
chr21:28992807-28993052 | Common:1; Rare:112 | ||||
chr21:29073529-29073848 | Common:2; Rare:100 | ||||
chr21:29298734-29298953 | Common:2; Rare:95 | ||||
chr21:31659531-31659837 | Common:2; Rare:131; Clinvar:5; Clinvar (benign):5; Clinvar (pathogenic):7 |