| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125261645-125261948 | Common:6; Rare:201 | ||||
| chr9:125672227-125672950 | Common:4; Rare:259 | ||||
| chr9:125707012-125707393 | Common:4; Rare:193 | ||||
| chr9:125747295-125747524 | Common:2; Rare:140 | ||||
| chr9:126804852-126805120 | Common:7; Rare:177 | ||||
| chr9:126805381-126805531 | Rare:36 | ||||
| chr9:126860544-126860933 | Common:7; Rare:152 | ||||
| chr9:126914655-126914861 | Common:2; Rare:72 | ||||
| chr9:127224348-127224654 | Rare:80 | ||||
| chr9:127245090-127245390 | Common:6; Rare:126 | ||||
| chr9:127396568-127397465 | Common:12; Rare:480 | ||||
| chr9:127424026-127424500 | Common:2; Rare:262 | ||||
| chr9:127450707-127450960 | Common:4; Rare:112 | ||||
| chr9:127451010-127451260 | Common:4; Rare:101 | ||||
| chr9:127451364-127451950 | Common:6; Rare:264; Clinvar:8; Clinvar (benign):3 |