Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:10673942-10674205 | Common:3; Rare:96; Clinvar:3; Clinvar (benign):3 | ||||
chr20:13784884-13785080 | Common:2; Rare:87; Clinvar (benign):3 | ||||
chr20:16573297-16573547 | Common:1; Rare:72 | ||||
chr20:17968438-17968590 | Common:4; Rare:63 | ||||
chr20:17968784-17969122 | Common:3; Rare:120 | ||||
chr20:18137779-18137947 | Common:1; Rare:61 | ||||
chr20:18467072-18467439 | Common:1; Rare:78 | ||||
chr20:19888929-19889248 | Common:1; Rare:52 | ||||
chr20:20017143-20017388 | Rare:74 | ||||
chr20:20712595-20712729 | Common:2; Rare:47 | ||||
chr20:21303261-21303464 | Rare:71 | ||||
chr20:23085728-23085884 | Common:2; Rare:48 | ||||
chr20:23086194-23086506 | Common:1; Rare:70 | ||||
chr20:24992671-24992833 | Common:4; Rare:74 | ||||
chr20:25195607-25195848 | Common:4; Rare:76 |