| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121834987-121835231 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383199-122383323 | Common:1; Rare:37 | ||||
| chr3:122383941-122384250 | Rare:102 | ||||
| chr3:122416039-122416225 | Common:1; Rare:61 | ||||
| chr3:122564235-122564452 | Common:3; Rare:67 | ||||
| chr3:123066940-123067172 | Rare:60 | ||||
| chr3:123404522-123404833 | Common:1; Rare:60 | ||||
| chr3:123649160-123649355 | Common:2; Rare:47; Clinvar:1; Clinvar (benign):10 | ||||
| chr3:123692349-123692474 | Rare:30 | ||||
| chr3:124730367-124730474 | Common:2; Rare:59; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:125375221-125375431 | Rare:63 | ||||
| chr3:125595248-125595664 | Common:3; Rare:120 | ||||
| chr3:126101490-126101625 | Common:1; Rare:24 | ||||
| chr3:126180510-126180590 | Rare:10 | ||||
| chr3:126704074-126704284 | Common:2; Rare:61 |