| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123961182-123961310 | Rare:56 | ||||
| chr3:124730340-124730468 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:125375242-125375458 | Rare:63 | ||||
| chr3:125520162-125520319 | Rare:44 | ||||
| chr3:125595284-125595530 | Common:2; Rare:65 | ||||
| chr3:126704001-126704271 | Common:3; Rare:75 | ||||
| chr3:127598202-127598491 | Common:3; Rare:93 | ||||
| chr3:127736127-127736311 | Common:2; Rare:26 | ||||
| chr3:128052196-128052517 | Common:2; Rare:106 | ||||
| chr3:128123753-128124051 | Rare:81 | ||||
| chr3:128680981-128681231 | Common:1; Rare:65 | ||||
| chr3:128726020-128726175 | Common:1; Rare:40; Clinvar:2 | ||||
| chr3:128879369-128879675 | Common:5; Rare:144; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129160991-129161169 | Common:1; Rare:70 | ||||
| chr3:129183814-129184113 | Common:2; Rare:112 |