| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121749131-121749298 | Rare:28 | ||||
| chr3:121749422-121749522 | Rare:18 | ||||
| chr3:121749623-121750021 | Common:1; Rare:91 | ||||
| chr3:121834956-121835244 | Common:3; Rare:95; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383184-122383332 | Common:1; Rare:45 | ||||
| chr3:122384074-122384291 | Common:3; Rare:80 | ||||
| chr3:122416039-122416229 | Common:1; Rare:61 | ||||
| chr3:122416448-122416550 | Common:1; Rare:21 | ||||
| chr3:122514800-122515029 | Common:2; Rare:63 | ||||
| chr3:122564205-122564437 | Common:3; Rare:63 | ||||
| chr3:122680713-122680913 | Rare:65 | ||||
| chr3:123201839-123201978 | Common:1; Rare:46 | ||||
| chr3:123584986-123585257 | Common:1; Rare:93 | ||||
| chr3:123585484-123585582 | Rare:16 | ||||
| chr3:123692310-123692641 | Rare:72 |