Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr8:6406518-6406676 | Common:3; Rare:85; Clinvar:2; Clinvar (benign):1 | ||||
chr8:10839793-10839961 | Rare:69 | ||||
chr8:11284740-11284860 | Common:2; Rare:54 | ||||
chr8:11474677-11474871 | Common:3; Rare:46 | ||||
chr8:11802440-11802792 | Common:6; Rare:191 | ||||
chr8:11845696-11845909 | Rare:135 | ||||
chr8:15540182-15540336 | Common:2; Rare:58; Clinvar:7; Clinvar (benign):1 | ||||
chr8:17246591-17247084 | Common:5; Rare:203 | ||||
chr8:17922616-17923068 | Common:5; Rare:174 | ||||
chr8:18084939-18085027 | Rare:18 | ||||
chr8:19013657-19013961 | Common:4; Rare:87 | ||||
chr8:19313563-19313772 | Common:3; Rare:62 | ||||
chr8:22245023-22245192 | Common:1; Rare:83 | ||||
chr8:23164006-23164227 | Rare:46 | ||||
chr8:23404105-23404327 | Common:2; Rare:58 |