Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:88856923-88857175 | Common:4; Rare:115; Clinvar:1; Clinvar (benign):2 | ||||
chr16:89217619-89217712 | Common:1; Rare:42 | ||||
chr16:89508280-89508443 | Common:1; Rare:93; Clinvar:2; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
chr16:89560541-89560717 | Rare:73 | ||||
chr16:89657647-89657846 | Common:1; Rare:100 | ||||
chr16:89972521-89972648 | Rare:47 | ||||
chr16:90022555-90022709 | Rare:60 | ||||
chr17:714802-714899 | Common:1; Rare:34 | ||||
chr17:1516605-1516949 | Rare:118 | ||||
chr17:1762817-1762823 | Rare:1 | ||||
chr17:1829832-1830039 | Common:6; Rare:87 | ||||
chr17:2214291-2214420 | Common:1; Rare:21 | ||||
chr17:2303488-2303633 | Rare:52 | ||||
chr17:2303766-2303987 | Common:2; Rare:80 | ||||
chr17:2336430-2336490 | Rare:20 |