Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr5:36151819-36152174 | Rare:99 | ||||
chr5:36241588-36241959 | Common:4; Rare:132; Clinvar:1; Clinvar (benign):4 | ||||
chr5:36242126-36242458 | Common:3; Rare:93 | ||||
chr5:36876650-36876915 | Common:1; Rare:80; Clinvar:1; Clinvar (benign):1 | ||||
chr5:36876949-36877173 | Rare:70; Clinvar:2; Clinvar (benign):2 | ||||
chr5:37371018-37371189 | Rare:67 | ||||
chr5:37379156-37379364 | Common:1; Rare:51 | ||||
chr5:38445281-38445561 | Common:1; Rare:50 | ||||
chr5:38556458-38556809 | Common:3; Rare:119 | ||||
chr5:38557183-38557294 | Rare:25 | ||||
chr5:38557458-38557535 | Rare:15 | ||||
chr5:38845712-38846053 | Common:2; Rare:89 | ||||
chr5:39074327-39074505 | Common:1; Rare:84 | ||||
chr5:40679303-40679425 | Common:1; Rare:23 | ||||
chr5:40679745-40679971 | Rare:50 |