| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:144852970-144853143 | Rare:63 | ||||
| chr8:144901376-144901594 | Common:1; Rare:66 | ||||
| chr8:144950814-144950890 | Common:1; Rare:23 | ||||
| chr8:145052145-145052518 | Common:11; Rare:100 | ||||
| chr9:178997-179102 | Common:2; Rare:18 | ||||
| chr9:2015034-2015387 | Common:3; Rare:105 | ||||
| chr9:2017325-2017441 | Rare:28 | ||||
| chr9:2017483-2017718 | Rare:71 | ||||
| chr9:2157341-2157674 | Common:3; Rare:82 | ||||
| chr9:2158138-2158493 | Common:1; Rare:75 | ||||
| chr9:2621837-2622169 | Common:4; Rare:112; Clinvar:7; Clinvar (benign):2 | ||||
| chr9:2844049-2844367 | Common:6; Rare:126 | ||||
| chr9:3525477-3525593 | Rare:48 | ||||
| chr9:3525763-3526106 | Common:1; Rare:121 | ||||
| chr9:3526370-3526521 | Common:5; Rare:78 |