| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr9:121326477-121326770 | Common:3; Rare:104; Clinvar:3; Clinvar (benign):5 | ||||
| chr9:121370175-121370453 | Common:2; Rare:81 | ||||
| chr9:122159708-122159880 | Rare:71 | ||||
| chr9:122264408-122264691 | Common:2; Rare:57 | ||||
| chr9:122264713-122264922 | Common:3; Rare:57 | ||||
| chr9:122913271-122913395 | Common:2; Rare:24 | ||||
| chr9:122931482-122931689 | Common:3; Rare:41 | ||||
| chr9:124861890-124862153 | Common:1; Rare:116 | ||||
| chr9:124940964-124941168 | Common:3; Rare:70 | ||||
| chr9:125189733-125190031 | Common:1; Rare:139 | ||||
| chr9:125200431-125200590 | Common:1; Rare:57 | ||||
| chr9:125241282-125241686 | Common:3; Rare:123 | ||||
| chr9:125261645-125261860 | Common:2; Rare:78 | ||||
| chr9:126804962-126805064 | Common:1; Rare:32 | ||||
| chr9:127424111-127424450 | Common:1; Rare:95 |