| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:120742503-120742783 | Common:2; Rare:78 | ||||
| chr3:121749233-121749300 | Rare:17 | ||||
| chr3:121749463-121749528 | Rare:13 | ||||
| chr3:121749643-121750025 | Common:1; Rare:88 | ||||
| chr3:121834987-121835234 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383180-122383345 | Common:2; Rare:50 | ||||
| chr3:122384036-122384247 | Rare:77 | ||||
| chr3:122416039-122416225 | Common:1; Rare:61 | ||||
| chr3:122514878-122515026 | Common:1; Rare:38 | ||||
| chr3:122564236-122564437 | Common:3; Rare:59 | ||||
| chr3:123201636-123201979 | Common:1; Rare:91 | ||||
| chr3:123584980-123585317 | Common:1; Rare:108 | ||||
| chr3:123585504-123585590 | Rare:17 | ||||
| chr3:123961221-123961497 | Common:3; Rare:108 | ||||
| chr3:124227288-124227603 | Common:3; Rare:42 |