| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:127737627-127737783 | Common:1; Rare:45 | ||||
| chr8:144431178-144431413 | Common:4; Rare:53 | ||||
| chr8:145002844-145003038 | Common:2; Rare:64 | ||||
| chr9:32550829-32551135 | Common:1; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr9:40991976-40992399 | Common:7; Rare:30 | ||||
| chr9:62897703-62897780 | Rare:25 | ||||
| chr9:70205875-70205930 | Rare:9 | ||||
| chr9:70418989-70419205 | Common:2; Rare:55 | ||||
| chr9:71769464-71769722 | Rare:51 | ||||
| chr9:72305195-72305454 | Common:2; Rare:41 | ||||
| chr9:83219209-83219345 | Common:2; Rare:35 | ||||
| chr9:96686979-96687057 | Common:1; Rare:20 | ||||
| chr9:108551596-108551733 | Rare:28 | ||||
| chr9:136726207-136726319 | Common:2; Rare:41 | ||||
| chr9:136863447-136863608 | Rare:34 |