Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr18:31329820-31329963 | Rare:31; Clinvar (pathogenic):1 | ||||
chr18:31342523-31342626 | Common:2; Rare:18 | ||||
chr18:31345720-31346017 | Rare:59 | ||||
chr18:31354090-31354520 | Common:9; Rare:121 | ||||
chr18:31426854-31427001 | Rare:21 | ||||
chr18:31451735-31452046 | Common:3; Rare:50 | ||||
chr18:31462316-31462577 | Common:1; Rare:50 | ||||
chr18:63478118-63478264 | Common:3; Rare:32 | ||||
chr18:63593571-63593743 | Common:2; Rare:27 | ||||
chr18:76487716-76487919 | Common:2; Rare:42 | ||||
chr19:3977213-3977610 | Common:4; Rare:130; Clinvar (benign):8 | ||||
chr19:5550007-5550262 | Common:3; Rare:60 | ||||
chr19:5551969-5552235 | Common:1; Rare:46 | ||||
chr19:6742804-6743061 | Common:1; Rare:64 | ||||
chr19:6744379-6744634 | Common:1; Rare:78 |