| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122384084-122384292 | Common:3; Rare:74 | ||||
| chr3:122416068-122416225 | Rare:47 | ||||
| chr3:122564231-122564429 | Common:3; Rare:58 | ||||
| chr3:123201863-123201967 | Common:1; Rare:35 | ||||
| chr3:124584582-124584874 | Rare:78 | ||||
| chr3:124730340-124730468 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:125375236-125375593 | Common:1; Rare:100 | ||||
| chr3:126084091-126084270 | Common:1; Rare:76 | ||||
| chr3:126179888-126180080 | Common:1; Rare:51 | ||||
| chr3:126180510-126180679 | Common:1; Rare:35 | ||||
| chr3:127598223-127598432 | Common:3; Rare:52 | ||||
| chr3:127823169-127823365 | Common:3; Rare:40 | ||||
| chr3:128052147-128052532 | Common:3; Rare:128 | ||||
| chr3:128153365-128153509 | Rare:45 | ||||
| chr3:128879408-128879696 | Common:4; Rare:141; Clinvar:2; Clinvar (benign):3; Clinvar (pathogenic):1 |