Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:70205648-70205776 | Common:3; Rare:55; Clinvar (benign):2 | ||||
chr18:74148321-74148555 | Common:2; Rare:85 | ||||
chr18:74291902-74292253 | Common:3; Rare:100 | ||||
chr18:74597801-74597881 | Common:1; Rare:22 | ||||
chr18:79988402-79988593 | Common:2; Rare:78 | ||||
chr19:572237-572610 | Common:3; Rare:179 | ||||
chr19:633525-633715 | Common:8; Rare:86 | ||||
chr19:893167-893480 | Common:3; Rare:128 | ||||
chr19:984274-984378 | Rare:35 | ||||
chr19:1026488-1026680 | Rare:75 | ||||
chr19:1103749-1104115 | Common:7; Rare:153 | ||||
chr19:1401488-1401682 | Common:2; Rare:59; Clinvar:1; Clinvar (benign):4 | ||||
chr19:1438255-1438438 | Rare:68 | ||||
chr19:2328559-2328696 | Rare:66 | ||||
chr19:3572631-3572984 | Common:2; Rare:100 |