| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:119677374-119677524 | Rare:49 | ||||
| chr3:120742506-120742791 | Common:2; Rare:81 | ||||
| chr3:121545962-121546080 | Common:1; Rare:33 | ||||
| chr3:121660814-121660993 | Rare:38 | ||||
| chr3:121749640-121749795 | Rare:35 | ||||
| chr3:121834952-121835251 | Common:3; Rare:103; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122416039-122416231 | Common:1; Rare:61 | ||||
| chr3:122514774-122515029 | Common:3; Rare:70 | ||||
| chr3:122564130-122564427 | Common:4; Rare:86 | ||||
| chr3:122794849-122795069 | Rare:67 | ||||
| chr3:123201779-123202020 | Common:2; Rare:83 | ||||
| chr3:123585025-123585322 | Common:1; Rare:94 | ||||
| chr3:123585498-123585590 | Rare:19 | ||||
| chr3:125375249-125375425 | Rare:53 | ||||
| chr3:125520170-125520297 | Rare:32 |