Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:33993078-33993291 | Rare:57 | ||||
chr20:33994022-33994124 | Rare:31 | ||||
chr20:34112106-34112441 | Rare:111 | ||||
chr20:34303267-34303399 | Common:2; Rare:72; Clinvar:3; Clinvar (benign):2 | ||||
chr20:34516331-34516443 | Rare:41 | ||||
chr20:34558518-34558719 | Common:1; Rare:53 | ||||
chr20:34677078-34677324 | Rare:64 | ||||
chr20:34872820-34872965 | Rare:52 | ||||
chr20:34876283-34876665 | Common:3; Rare:103 | ||||
chr20:34955743-34955905 | Common:1; Rare:64; Clinvar:2; Clinvar (benign):2 | ||||
chr20:35147271-35147628 | Common:1; Rare:82 | ||||
chr20:35278034-35278218 | Common:3; Rare:66 | ||||
chr20:35284728-35284903 | Common:1; Rare:57 | ||||
chr20:35411959-35412137 | Rare:64 | ||||
chr20:35455059-35455210 | Common:1; Rare:54 |