Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:11890622-11890854 | Common:2; Rare:74 | ||||
chr20:13784893-13785053 | Common:2; Rare:65; Clinvar (benign):2 | ||||
chr20:16729821-16730063 | Common:2; Rare:76 | ||||
chr20:17968438-17968594 | Common:4; Rare:65 | ||||
chr20:17968789-17968956 | Common:2; Rare:70 | ||||
chr20:18507418-18507590 | Common:1; Rare:45 | ||||
chr20:18567339-18567491 | Common:1; Rare:57 | ||||
chr20:21303261-21303381 | Rare:55 | ||||
chr20:23350488-23350861 | Common:4; Rare:116 | ||||
chr20:32207724-32207939 | Common:3; Rare:82 | ||||
chr20:33401491-33401588 | Rare:25 | ||||
chr20:34112185-34112430 | Rare:74 | ||||
chr20:35092787-35092877 | Rare:50 | ||||
chr20:35284545-35284903 | Common:2; Rare:94 | ||||
chr20:35455051-35455214 | Common:1; Rare:58 |