| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr16:30534712-30535102 | Common:3; Rare:124 | ||||
| chr16:30585537-30585902 | Common:1; Rare:82 | ||||
| chr16:30650815-30651010 | Rare:65 | ||||
| chr16:30698446-30698644 | Common:1; Rare:77 | ||||
| chr16:30698997-30699364 | Rare:100; Clinvar (benign):1 | ||||
| chr16:30762079-30762343 | Common:3; Rare:89 | ||||
| chr16:30893940-30894275 | Common:5; Rare:91 | ||||
| chr16:30896500-30896635 | Common:1; Rare:36 | ||||
| chr16:30923251-30923592 | Common:1; Rare:84 | ||||
| chr16:30948988-30949120 | Rare:27 | ||||
| chr16:30997296-30997447 | Common:1; Rare:33 | ||||
| chr16:31033233-31033783 | Common:2; Rare:149 | ||||
| chr16:31073726-31073838 | Rare:35 | ||||
| chr16:31074187-31074456 | Common:1; Rare:75 | ||||
| chr16:31108292-31108458 | Rare:39 |