| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122795501-122795606 | Rare:35 | ||||
| chr3:123585489-123585553 | Rare:11 | ||||
| chr3:125375224-125375378 | Rare:42 | ||||
| chr3:125594772-125595115 | Common:3; Rare:85 | ||||
| chr3:125595214-125595500 | Common:2; Rare:78 | ||||
| chr3:125595508-125595664 | Common:1; Rare:50 | ||||
| chr3:126084103-126084241 | Common:1; Rare:63 | ||||
| chr3:126180510-126180818 | Common:1; Rare:69 | ||||
| chr3:126180854-126181018 | Common:1; Rare:51 | ||||
| chr3:127598223-127598446 | Common:3; Rare:59 | ||||
| chr3:127628949-127629205 | Common:1; Rare:84 | ||||
| chr3:127915467-127915579 | Common:2; Rare:23 | ||||
| chr3:128153370-128153496 | Rare:36 | ||||
| chr3:128879408-128879694 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 | ||||
| chr3:129183753-129184079 | Common:3; Rare:108 |