| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123884184-123884443 | Common:4; Rare:84; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:123949568-123949776 | Common:2; Rare:35 | ||||
| chr3:123960857-123961036 | Common:1; Rare:42 | ||||
| chr3:123961075-123961154 | Rare:28 | ||||
| chr3:124730342-124730612 | Common:4; Rare:121; Clinvar:5; Clinvar (benign):4 | ||||
| chr3:124886948-124887240 | Common:1; Rare:83 | ||||
| chr3:125055636-125055766 | Common:1; Rare:34 | ||||
| chr3:125375110-125375392 | Rare:69 | ||||
| chr3:125520014-125520392 | Rare:120 | ||||
| chr3:125594738-125594840 | Rare:36 | ||||
| chr3:126083986-126084199 | Common:2; Rare:64 | ||||
| chr3:126704114-126704360 | Common:2; Rare:85 | ||||
| chr3:127590479-127590707 | Common:2; Rare:57 | ||||
| chr3:127590711-127590918 | Common:2; Rare:45 | ||||
| chr3:127598209-127598461 | Common:3; Rare:74 |