| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:123066873-123067167 | Rare:71 | ||||
| chr3:123201720-123202051 | Common:2; Rare:96 | ||||
| chr3:123585028-123585394 | Common:1; Rare:117 | ||||
| chr3:123585491-123585666 | Rare:30 | ||||
| chr3:123700997-123701108 | Rare:23; Clinvar:1 | ||||
| chr3:123949591-123949679 | Rare:12 | ||||
| chr3:123949761-123949805 | Rare:6 | ||||
| chr3:123961184-123961497 | Common:3; Rare:126 | ||||
| chr3:124730340-124730608 | Common:4; Rare:120; Clinvar:5; Clinvar (benign):4 | ||||
| chr3:124887232-124887737 | Common:4; Rare:164 | ||||
| chr3:125056009-125056234 | Rare:65 | ||||
| chr3:125357253-125357338 | Common:1; Rare:28 | ||||
| chr3:125375120-125375431 | Rare:87 | ||||
| chr3:125520111-125520298 | Rare:70 | ||||
| chr3:125595437-125595756 | Common:2; Rare:92 |