Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr19:37932488-37932652 | Common:2; Rare:31 | ||||
chr19:38264271-38264659 | Common:6; Rare:101 | ||||
chr19:38374419-38374826 | Rare:158 | ||||
chr19:38899572-38900039 | Rare:138 | ||||
chr19:38930742-38930987 | Common:2; Rare:64; Clinvar:2; Clinvar (benign):3 | ||||
chr19:39391057-39391425 | Common:1; Rare:152 | ||||
chr19:39406699-39406873 | Rare:68 | ||||
chr19:39480608-39480912 | Common:3; Rare:152; Clinvar (pathogenic):1 | ||||
chr19:39970880-39971196 | Common:5; Rare:89 | ||||
chr19:40056157-40056288 | Rare:18 | ||||
chr19:40348377-40348739 | Common:4; Rare:121 | ||||
chr19:40377813-40378080 | Common:2; Rare:102; Clinvar (benign):1 | ||||
chr19:40425990-40426147 | Common:1; Rare:45 | ||||
chr19:40465700-40466011 | Common:2; Rare:99 | ||||
chr19:40717219-40717358 | Common:1; Rare:46 |