Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:31189153-31189287 | Rare:28; Clinvar (pathogenic):1 | ||||
chr16:72664962-72665170 | Rare:67 | ||||
chr16:74368137-74368407 | Common:1; Rare:72 | ||||
chr16:75000904-75001169 | Common:1; Rare:76 | ||||
chr16:75043113-75043182 | Rare:14 | ||||
chr16:79770298-79770433 | Common:2; Rare:46 | ||||
chr16:81632768-81632980 | Common:1; Rare:41 | ||||
chr16:81634822-81635032 | Rare:35 | ||||
chr16:85554261-85554308 | Rare:12 | ||||
chr16:85555255-85555759 | Common:1; Rare:128 | ||||
chr16:88790725-88790866 | Rare:44 | ||||
chr16:88793697-88793829 | Common:9; Rare:33 | ||||
chr16:88800004-88800311 | Common:5; Rare:80 | ||||
chr16:89115215-89115582 | Common:3; Rare:86 | ||||
chr17:503122-503180 | Common:1; Rare:9 |