| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:125241304-125241625 | Common:2; Rare:98 | ||||
| chr9:125261716-125261854 | Common:1; Rare:49 | ||||
| chr9:126805349-126805394 | Rare:8 | ||||
| chr9:126860589-126860678 | Common:2; Rare:28 | ||||
| chr9:127122613-127122850 | Common:2; Rare:60 | ||||
| chr9:127397193-127397211 | Rare:10 | ||||
| chr9:127424270-127424499 | Common:1; Rare:74 | ||||
| chr9:127449610-127449939 | Rare:90 | ||||
| chr9:127450084-127450320 | Common:1; Rare:54 | ||||
| chr9:127451067-127451165 | Common:1; Rare:31 | ||||
| chr9:127451257-127451580 | Common:3; Rare:130; Clinvar (benign):1 | ||||
| chr9:127937824-127937932 | Common:1; Rare:28; Clinvar:1; Clinvar (benign):1 | ||||
| chr9:128098181-128098580 | Common:3; Rare:88 | ||||
| chr9:128167822-128167854 | Rare:7 | ||||
| chr9:128191444-128191668 | Rare:67 |