| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:19230358-19230833 | Common:8; Rare:206 | ||||
| chr9:19380165-19380320 | Common:4; Rare:83 | ||||
| chr9:20684103-20684283 | Common:3; Rare:71 | ||||
| chr9:21335347-21335526 | Common:3; Rare:68 | ||||
| chr9:26892404-26892503 | Rare:45 | ||||
| chr9:26892736-26892874 | Rare:68 | ||||
| chr9:26947117-26947281 | Rare:62 | ||||
| chr9:26947408-26947566 | Common:1; Rare:50 | ||||
| chr9:26956293-26956470 | Common:2; Rare:63 | ||||
| chr9:27109020-27109258 | Common:1; Rare:62; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:27529738-27529920 | Common:4; Rare:57 | ||||
| chr9:27573417-27573524 | Common:6; Rare:55 | ||||
| chr9:27573709-27573908 | Common:2; Rare:63; Clinvar:5; Clinvar (benign):1 | ||||
| chr9:32384478-32384726 | Common:1; Rare:90 | ||||
| chr9:32573073-32573224 | Common:3; Rare:55 |