| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144517818-144518030 | Common:1; Rare:66 | ||||
| chr8:144792356-144792590 | Common:2; Rare:92 | ||||
| chr8:144827234-144827596 | Common:2; Rare:91 | ||||
| chr8:144901416-144901731 | Common:1; Rare:89 | ||||
| chr9:706953-707154 | Common:3; Rare:64 | ||||
| chr9:2844051-2844320 | Common:5; Rare:100 | ||||
| chr9:4490344-4490508 | Common:1; Rare:58; Clinvar:2 | ||||
| chr9:4662259-4662389 | Common:3; Rare:58 | ||||
| chr9:4679434-4679715 | Common:1; Rare:123 | ||||
| chr9:6015600-6015732 | Rare:57 | ||||
| chr9:20684096-20684285 | Common:3; Rare:76 | ||||
| chr9:21994192-21994797 | Common:2; Rare:191; Clinvar:16; Clinvar (benign):15; Clinvar (pathogenic):2 | ||||
| chr9:21994928-21995104 | Common:1; Rare:29 | ||||
| chr9:26892706-26892877 | Rare:84 | ||||
| chr9:26947135-26947261 | Rare:46 |