Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:31692030-31692199 | Common:1; Rare:31 | ||||
chr20:32018122-32018279 | Common:9; Rare:51 | ||||
chr20:32188120-32188406 | Rare:56 | ||||
chr20:32190284-32190493 | Common:2; Rare:43 | ||||
chr20:32781150-32781529 | Common:4; Rare:89; Clinvar:4; Clinvar (benign):2 | ||||
chr20:32785685-32785856 | Rare:25 | ||||
chr20:32787868-32787959 | Rare:21 | ||||
chr20:32788819-32789112 | Rare:57; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr20:32793541-32793675 | Rare:36 | ||||
chr20:32794282-32794322 | Rare:5 | ||||
chr20:32797129-32797231 | Common:1; Rare:25; Clinvar (benign):1 | ||||
chr20:32802528-32802612 | Rare:10 | ||||
chr20:32803892-32804118 | Common:3; Rare:37 | ||||
chr20:32804504-32804674 | Common:1; Rare:35 | ||||
chr20:32805088-32805417 | Common:2; Rare:78; Clinvar:2; Clinvar (pathogenic):1 |