| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:487560-487704 | Rare:27 | ||||
| chr9:533360-533608 | Rare:68 | ||||
| chr9:580397-580591 | Rare:65 | ||||
| chr9:637350-637525 | Common:2; Rare:41 | ||||
| chr9:843224-843347 | Rare:44 | ||||
| chr9:967837-968136 | Common:6; Rare:101 | ||||
| chr9:971861-972168 | Common:3; Rare:114 | ||||
| chr9:1476969-1477048 | Common:4; Rare:44 | ||||
| chr9:2718346-2718479 | Common:2; Rare:90; Clinvar:2; Clinvar (benign):3 | ||||
| chr9:3526696-3526767 | Rare:27 | ||||
| chr9:3668033-3668165 | Rare:25 | ||||
| chr9:3734262-3734566 | Common:2; Rare:83 | ||||
| chr9:4196164-4196384 | Common:1; Rare:68 | ||||
| chr9:5630096-5630239 | Common:1; Rare:42 | ||||
| chr9:5768935-5769007 | Rare:24 |