| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4272587-4272638 | Common:1; Rare:22 | ||||
| chr16:4272662-4272911 | Rare:62 | ||||
| chr16:4425763-4425892 | Common:1; Rare:63 | ||||
| chr16:4476304-4476481 | Common:1; Rare:67 | ||||
| chr16:4611038-4611328 | Common:2; Rare:55 | ||||
| chr16:4734159-4734542 | Common:1; Rare:125 | ||||
| chr16:4767140-4767322 | Common:1; Rare:59 | ||||
| chr16:4847230-4847484 | Common:2; Rare:116 | ||||
| chr16:5033920-5033955 | Rare:14 | ||||
| chr16:8797599-8797944 | Common:1; Rare:141; Clinvar:5; Clinvar (benign):2; Clinvar (pathogenic):5 | ||||
| chr16:8868977-8869227 | Common:4; Rare:114 | ||||
| chr16:10580561-10580722 | Rare:51 | ||||
| chr16:10743756-10743896 | Rare:52 | ||||
| chr16:11345231-11345469 | Common:1; Rare:79 | ||||
| chr16:11586887-11587274 | Common:4; Rare:89 |