| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:126558346-126558628 | Common:1; Rare:104 | ||||
| chr8:132675536-132675665 | Rare:36 | ||||
| chr8:140511231-140511509 | Common:3; Rare:107 | ||||
| chr8:141001144-141001496 | Common:4; Rare:124 | ||||
| chr8:141391899-141392073 | Common:1; Rare:58 | ||||
| chr8:143018260-143018545 | Common:2; Rare:76 | ||||
| chr8:144082503-144082670 | Common:2; Rare:58 | ||||
| chr8:144901408-144901712 | Common:1; Rare:85 | ||||
| chr8:145052193-145052497 | Common:10; Rare:84 | ||||
| chr9:2158234-2158480 | Rare:50 | ||||
| chr9:2621868-2622163 | Common:4; Rare:94; Clinvar:6; Clinvar (benign):2 | ||||
| chr9:2717747-2717750 | Rare:1 | ||||
| chr9:2844047-2844329 | Common:5; Rare:104 | ||||
| chr9:4679437-4679708 | Rare:119 | ||||
| chr9:13279616-13279811 | Common:2; Rare:61 |