| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121749639-121750031 | Common:1; Rare:91 | ||||
| chr3:121834955-121835235 | Common:3; Rare:90; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383174-122383369 | Common:2; Rare:59 | ||||
| chr3:122384016-122384268 | Rare:89 | ||||
| chr3:122416039-122416237 | Common:1; Rare:62 | ||||
| chr3:122514828-122515031 | Common:2; Rare:58 | ||||
| chr3:122564244-122564452 | Common:3; Rare:66 | ||||
| chr3:123066954-123067156 | Rare:51 | ||||
| chr3:123201731-123201980 | Common:1; Rare:78 | ||||
| chr3:123585023-123585284 | Common:1; Rare:83 | ||||
| chr3:123585502-123585648 | Rare:25 | ||||
| chr3:123961182-123961497 | Common:3; Rare:126 | ||||
| chr3:124730374-124730495 | Common:2; Rare:68; Clinvar:4; Clinvar (benign):2 | ||||
| chr3:125375133-125375431 | Rare:86 | ||||
| chr3:125520162-125520299 | Rare:39 |