| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:4624520-4624860 | Common:1; Rare:115 | ||||
| chr16:4625292-4625512 | Common:2; Rare:67 | ||||
| chr16:4693418-4693773 | Common:3; Rare:159 | ||||
| chr16:4734366-4734576 | Rare:64 | ||||
| chr16:4734807-4735015 | Common:1; Rare:70 | ||||
| chr16:4767129-4767355 | Common:1; Rare:75 | ||||
| chr16:4802603-4802801 | Rare:67; Clinvar:5 | ||||
| chr16:4847223-4847526 | Common:3; Rare:142 | ||||
| chr16:4957910-4958360 | Common:9; Rare:124 | ||||
| chr16:5033864-5034006 | Rare:62 | ||||
| chr16:5071778-5071911 | Rare:80; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr16:5072040-5072190 | Common:6; Rare:87; Clinvar:2; Clinvar (benign):5 | ||||
| chr16:5097794-5098589 | Common:5; Rare:280 | ||||
| chr16:8621585-8621788 | Common:1; Rare:83 | ||||
| chr16:8674363-8674661 | Common:2; Rare:105; Clinvar:2 |