| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:64561269-64561504 | Common:2; Rare:41 | ||||
| chr3:66398985-66399144 | Rare:54 | ||||
| chr3:73625460-73625799 | Rare:59 | ||||
| chr3:75435017-75435386 | Common:5; Rare:126 | ||||
| chr3:75641089-75641279 | Rare:29 | ||||
| chr3:101576981-101577162 | Common:1; Rare:47 | ||||
| chr3:101676254-101676503 | Common:2; Rare:85 | ||||
| chr3:107240577-107240729 | Rare:67 | ||||
| chr3:112639896-112639994 | Rare:28 | ||||
| chr3:112640384-112640459 | Rare:18 | ||||
| chr3:120448778-120449007 | Rare:39 | ||||
| chr3:123335216-123335524 | Common:2; Rare:65 | ||||
| chr3:123447484-123447568 | Common:1; Rare:31 | ||||
| chr3:123614327-123614545 | Common:1; Rare:44; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:123618640-123619034 | Rare:108; Clinvar:7; Clinvar (benign):3 |