| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121749473-121749770 | Common:1; Rare:69 | ||||
| chr3:121834987-121835244 | Common:3; Rare:87; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383178-122383345 | Common:2; Rare:51 | ||||
| chr3:122384030-122384275 | Common:2; Rare:85 | ||||
| chr3:122514848-122515026 | Common:2; Rare:51 | ||||
| chr3:122564270-122564417 | Common:1; Rare:43 | ||||
| chr3:122793678-122793908 | Common:4; Rare:70 | ||||
| chr3:123585035-123585314 | Common:1; Rare:84 | ||||
| chr3:123585494-123585553 | Rare:10 | ||||
| chr3:124730322-124730474 | Common:3; Rare:82; Clinvar:2; Clinvar (benign):3 | ||||
| chr3:124887595-124887750 | Common:4; Rare:52 | ||||
| chr3:125375237-125375432 | Rare:60 | ||||
| chr3:125520111-125520391 | Rare:90 | ||||
| chr3:126703946-126704302 | Common:4; Rare:108 | ||||
| chr3:127598212-127598472 | Common:3; Rare:82 |