| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:128765213-128765263 | Rare:4 | ||||
| chr3:128801314-128801403 | Rare:19 | ||||
| chr3:129252349-129252643 | Common:1; Rare:62 | ||||
| chr3:129314787-129314894 | Common:1; Rare:31 | ||||
| chr3:129315272-129315303 | Rare:10 | ||||
| chr3:129386998-129387112 | Rare:21 | ||||
| chr3:129723784-129723831 | Rare:7 | ||||
| chr3:129723959-129724346 | Common:1; Rare:65 | ||||
| chr3:129794423-129794657 | Rare:35 | ||||
| chr3:129847985-129848205 | Rare:59 | ||||
| chr3:130959183-130959344 | Rare:38 | ||||
| chr3:130960384-130960648 | Common:2; Rare:51 | ||||
| chr3:130960691-130960909 | Common:1; Rare:29 | ||||
| chr3:130975232-130975529 | Common:2; Rare:71; Clinvar (benign):1; Clinvar (pathogenic):1 | ||||
| chr3:130991487-130991704 | Common:2; Rare:36 |