Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:66366506-66366724 | Common:3; Rare:44 | ||||
chr16:66552537-66552682 | Rare:60 | ||||
chr16:66727763-66727857 | Rare:19 | ||||
chr16:66923851-66924002 | Rare:26 | ||||
chr16:66934347-66934524 | Common:1; Rare:68 | ||||
chr16:66935366-66935655 | Rare:110 | ||||
chr16:67028992-67029116 | Rare:39 | ||||
chr16:67159885-67160023 | Rare:23 | ||||
chr16:67183548-67183628 | Rare:20 | ||||
chr16:67183948-67184011 | Common:1; Rare:20 | ||||
chr16:67227008-67227187 | Rare:75 | ||||
chr16:67481037-67481369 | Common:1; Rare:121 | ||||
chr16:67528751-67528856 | Rare:25 | ||||
chr16:67538558-67538750 | Common:1; Rare:85 | ||||
chr16:67660222-67660380 | Rare:94; Clinvar:2; Clinvar (benign):2 |