| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123700785-123701337 | Common:2; Rare:143; Clinvar:15; Clinvar (benign):10 | ||||
| chr3:123701436-123701626 | Common:1; Rare:63; Clinvar:7 | ||||
| chr3:123961221-123961531 | Common:3; Rare:117 | ||||
| chr3:124584562-124584780 | Rare:51 | ||||
| chr3:124730376-124730474 | Common:2; Rare:53; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:125357237-125357381 | Common:1; Rare:42 | ||||
| chr3:125375113-125375431 | Rare:87 | ||||
| chr3:125595258-125595375 | Common:2; Rare:39 | ||||
| chr3:125595522-125595725 | Rare:65 | ||||
| chr3:126056671-126056869 | Common:1; Rare:44 | ||||
| chr3:126084004-126084219 | Common:2; Rare:77 | ||||
| chr3:126179914-126180095 | Common:1; Rare:46 | ||||
| chr3:126180510-126180817 | Common:1; Rare:69 | ||||
| chr3:126180854-126180896 | Common:1; Rare:7 | ||||
| chr3:126181031-126181136 | Rare:23 |