| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:46689464-46689768 | Common:2; Rare:123; Clinvar:1; Clinvar (benign):2; Clinvar (pathogenic):1 | ||||
| chr16:46689854-46689980 | Rare:32 | ||||
| chr16:46690105-46690277 | Rare:40 | ||||
| chr16:46691012-46691106 | Rare:36; Clinvar:2 | ||||
| chr16:46789920-46790125 | Common:5; Rare:51 | ||||
| chr16:46830306-46830778 | Common:2; Rare:106 | ||||
| chr16:46830890-46831326 | Common:2; Rare:151 | ||||
| chr16:46831336-46831610 | Common:1; Rare:77 | ||||
| chr16:46883814-46884452 | Common:3; Rare:162 | ||||
| chr16:46972636-46972693 | Common:1; Rare:12 | ||||
| chr16:46972898-46973384 | Common:1; Rare:131 | ||||
| chr16:46973537-46974014 | Common:1; Rare:165 | ||||
| chr16:47143431-47143652 | Rare:61 | ||||
| chr16:47143731-47144157 | Common:1; Rare:172 | ||||
| chr16:47144191-47144332 | Rare:34 |