| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:121834987-121835231 | Common:3; Rare:81; Clinvar:6; Clinvar (benign):2 | ||||
| chr3:122383192-122383312 | Common:1; Rare:39 | ||||
| chr3:122384046-122384247 | Rare:76 | ||||
| chr3:122514880-122515006 | Common:1; Rare:35 | ||||
| chr3:123585035-123585317 | Common:1; Rare:85 | ||||
| chr3:124730371-124730468 | Common:2; Rare:51; Clinvar:1; Clinvar (benign):2 | ||||
| chr3:125375251-125375429 | Rare:54 | ||||
| chr3:125520163-125520271 | Rare:33 | ||||
| chr3:126704081-126704279 | Common:2; Rare:56 | ||||
| chr3:127598212-127598451 | Common:3; Rare:66 | ||||
| chr3:128879408-128879669 | Common:4; Rare:126; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183814-129184058 | Common:2; Rare:79 | ||||
| chr3:129278761-129278892 | Common:4; Rare:43 | ||||
| chr3:129316272-129316407 | Common:1; Rare:41 | ||||
| chr3:129439876-129440301 | Common:1; Rare:126; Clinvar:1; Clinvar (benign):1 |