| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:3717509-3717627 | Rare:61 | ||||
| chr16:4425773-4425880 | Common:1; Rare:50 | ||||
| chr16:4476290-4476473 | Common:1; Rare:70 | ||||
| chr16:4734167-4734542 | Common:1; Rare:124 | ||||
| chr16:4847258-4847436 | Common:1; Rare:75 | ||||
| chr16:5033920-5033955 | Rare:14 | ||||
| chr16:8797612-8797926 | Common:1; Rare:128; Clinvar:3; Clinvar (benign):2; Clinvar (pathogenic):4 | ||||
| chr16:11846530-11846789 | Common:1; Rare:84 | ||||
| chr16:11851511-11851645 | Rare:65 | ||||
| chr16:11915370-11915667 | Common:5; Rare:108 | ||||
| chr16:11976606-11976748 | Common:3; Rare:54 | ||||
| chr16:14071307-14071368 | Common:1; Rare:26 | ||||
| chr16:15888569-15888816 | Common:3; Rare:90 | ||||
| chr16:19067455-19067664 | Common:5; Rare:77 | ||||
| chr16:20806432-20806636 | Rare:68 |