| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122564243-122564429 | Common:3; Rare:56 | ||||
| chr3:123066885-123067156 | Rare:67 | ||||
| chr3:123585028-123585317 | Common:1; Rare:89 | ||||
| chr3:123585510-123585646 | Rare:24 | ||||
| chr3:123961194-123961497 | Common:3; Rare:122 | ||||
| chr3:124730365-124730468 | Common:2; Rare:55; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:125375160-125375384 | Rare:60 | ||||
| chr3:125595262-125595383 | Common:2; Rare:38 | ||||
| chr3:126083989-126084289 | Common:2; Rare:107 | ||||
| chr3:127598220-127598446 | Common:3; Rare:61 | ||||
| chr3:127628970-127629211 | Common:1; Rare:79 | ||||
| chr3:127672824-127673002 | Common:1; Rare:83 | ||||
| chr3:128052173-128052473 | Common:2; Rare:101 | ||||
| chr3:128153383-128153493 | Rare:32 | ||||
| chr3:128879425-128879669 | Common:4; Rare:120; Clinvar:2; Clinvar (benign):2 |