| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr8:130358616-130358771 | Common:1; Rare:62 | ||||
| chr8:140645969-140646162 | Common:1; Rare:29 | ||||
| chr8:143927624-143927885 | Common:3; Rare:108; Clinvar:19; Clinvar (benign):3 | ||||
| chr8:145002827-145003035 | Common:2; Rare:71 | ||||
| chr9:5509596-5509930 | Common:4; Rare:60 | ||||
| chr9:11065008-11065259 | Common:2; Rare:83 | ||||
| chr9:12814338-12814698 | Common:6; Rare:81 | ||||
| chr9:14993148-14993318 | Common:5; Rare:73 | ||||
| chr9:16063000-16063237 | Common:2; Rare:57 | ||||
| chr9:16337430-16337662 | Rare:49 | ||||
| chr9:16726824-16726933 | Common:1; Rare:24 | ||||
| chr9:18490623-18490937 | Rare:65 | ||||
| chr9:21559828-21559932 | Rare:63 | ||||
| chr9:21581005-21581189 | Rare:35 | ||||
| chr9:21591642-21592029 | Common:2; Rare:91 |