| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:133256751-133257041 | Common:1; Rare:73; Clinvar:1; Clinvar (benign):2 | ||||
| chr8:144890318-144890491 | Common:1; Rare:31 | ||||
| chr8:145002858-145003038 | Common:1; Rare:60 | ||||
| chr9:4887710-4887746 | Rare:5 | ||||
| chr9:40106586-40106766 | Common:2; Rare:19 | ||||
| chr9:40991985-40992407 | Common:7; Rare:28 | ||||
| chr9:62376203-62376544 | |||||
| chr9:62376789-62376825 | |||||
| chr9:63817472-63817802 | Common:8; Rare:3 | ||||
| chr9:66269667-66270047 | Common:3; Rare:47 | ||||
| chr9:70413045-70413148 | Rare:17 | ||||
| chr9:70413930-70414056 | Rare:23 | ||||
| chr9:83920715-83920771 | Rare:13 | ||||
| chr9:86948472-86948735 | Common:1; Rare:71 | ||||
| chr9:108040709-108041010 | Common:1; Rare:59 |