Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr20:31723486-31723713 | Common:1; Rare:66 | ||||
chr20:31739107-31739367 | Common:1; Rare:67 | ||||
chr20:31845594-31845771 | Rare:38 | ||||
chr20:32207665-32207939 | Common:3; Rare:100 | ||||
chr20:33401481-33401607 | Rare:31 | ||||
chr20:33720210-33720583 | Common:4; Rare:89 | ||||
chr20:33993078-33993284 | Rare:55 | ||||
chr20:34112102-34112441 | Rare:112 | ||||
chr20:34303267-34303492 | Common:2; Rare:94; Clinvar:3; Clinvar (benign):2 | ||||
chr20:34677078-34677305 | Rare:58 | ||||
chr20:34955733-34955898 | Common:1; Rare:68; Clinvar:3; Clinvar (benign):2 | ||||
chr20:35147248-35147370 | Common:1; Rare:47 | ||||
chr20:35284545-35284870 | Common:2; Rare:86 | ||||
chr20:35307089-35307171 | Common:1; Rare:13 | ||||
chr20:35455049-35455341 | Common:1; Rare:98 |