| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:56610170-56610497 | Common:2; Rare:99 | ||||
| chr16:56728978-56729378 | Common:1; Rare:80 | ||||
| chr16:56732373-56732594 | Common:2; Rare:35 | ||||
| chr16:56732800-56733160 | Common:1; Rare:54 | ||||
| chr16:56860420-56860850 | Common:8; Rare:129 | ||||
| chr16:56869480-56869940 | Rare:267; Clinvar (pathogenic):5 | ||||
| chr16:56870104-56870504 | Common:1; Rare:120; Clinvar:3; Clinvar (pathogenic):1 | ||||
| chr16:56871230-56871510 | Common:2; Rare:46 | ||||
| chr16:56888734-56889175 | Common:8; Rare:128 | ||||
| chr16:56911710-56912220 | Common:11; Rare:316 | ||||
| chr16:56916524-56917010 | Common:3; Rare:148 | ||||
| chr16:56917103-56917308 | Rare:65 | ||||
| chr16:56919030-56919350 | Common:2; Rare:60 | ||||
| chr16:56931220-56931482 | Common:8; Rare:62 | ||||
| chr16:56946074-56946766 | Common:3; Rare:185 |