Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
---|---|---|---|---|---|
chr16:89508305-89508432 | Common:1; Rare:63; Clinvar:1; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
chr16:89560541-89560717 | Rare:73 | ||||
chr16:89657637-89658098 | Common:3; Rare:240 | ||||
chr16:89686567-89686713 | Common:6; Rare:69 | ||||
chr16:89686878-89687007 | Rare:57 | ||||
chr16:89701687-89701822 | Rare:52 | ||||
chr16:89720865-89721010 | Common:1; Rare:44 | ||||
chr16:89816621-89816769 | Common:2; Rare:69; Clinvar:2; Clinvar (benign):1 | ||||
chr16:89873490-89873826 | Common:3; Rare:154 | ||||
chr16:89923171-89923345 | Rare:63 | ||||
chr16:89972442-89972664 | Common:1; Rare:84 | ||||
chr16:90019392-90019701 | Common:5; Rare:92 | ||||
chr16:90022552-90022713 | Rare:64 | ||||
chr17:331501-331659 | Rare:49 | ||||
chr17:339015-339239 | Common:1; Rare:42 |