| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4846515-4846681 | Common:2; Rare:40 | ||||
| chr16:4847231-4847409 | Common:1; Rare:84 | ||||
| chr16:5033920-5033981 | Rare:24 | ||||
| chr16:8797610-8797937 | Common:1; Rare:135; Clinvar:4; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr16:8900856-8901052 | Common:1; Rare:68 | ||||
| chr16:10743756-10743897 | Rare:52 | ||||
| chr16:11586887-11587084 | Common:3; Rare:52 | ||||
| chr16:11587152-11587327 | Common:1; Rare:44 | ||||
| chr16:11742723-11742927 | Common:1; Rare:83 | ||||
| chr16:11782352-11782666 | Common:2; Rare:83 | ||||
| chr16:11782964-11783056 | Rare:12 | ||||
| chr16:11797134-11797592 | Common:4; Rare:176 | ||||
| chr16:11851414-11851675 | Common:1; Rare:138 | ||||
| chr16:11886469-11886929 | Rare:91 | ||||
| chr16:11915370-11915496 | Common:4; Rare:54 |