| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144502894-144503084 | Common:2; Rare:46 | ||||
| chr8:144503260-144503600 | Common:2; Rare:85 | ||||
| chr8:144503990-144504187 | Rare:48 | ||||
| chr8:144508937-144509099 | Rare:43 | ||||
| chr8:144517705-144518029 | Common:1; Rare:114; Clinvar:10; Clinvar (benign):2 | ||||
| chr8:144755461-144755640 | Common:1; Rare:64 | ||||
| chr8:144792340-144792577 | Common:3; Rare:92 | ||||
| chr8:144827265-144827600 | Common:1; Rare:87 | ||||
| chr8:144901414-144901729 | Common:1; Rare:89 | ||||
| chr8:144950593-144950685 | Common:1; Rare:26 | ||||
| chr8:145052198-145052497 | Common:10; Rare:83 | ||||
| chr9:272956-273061 | Common:1; Rare:29 | ||||
| chr9:470010-470320 | Common:17; Rare:125 | ||||
| chr9:504391-504738 | Common:4; Rare:169 | ||||
| chr9:2015077-2015389 | Common:3; Rare:89 |