| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122564577-122564611 | Rare:11 | ||||
| chr3:122680670-122680952 | Rare:90 | ||||
| chr3:122681161-122681226 | Rare:14 | ||||
| chr3:123585023-123585284 | Common:1; Rare:83 | ||||
| chr3:123585489-123585590 | Rare:20 | ||||
| chr3:123692320-123692464 | Rare:33 | ||||
| chr3:123700969-123701315 | Rare:71; Clinvar:3; Clinvar (benign):1 | ||||
| chr3:123799933-123800097 | Common:2; Rare:43 | ||||
| chr3:124584584-124584772 | Rare:43 | ||||
| chr3:124730362-124730481 | Common:2; Rare:66; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:125375114-125375431 | Rare:87 | ||||
| chr3:125520129-125520313 | Rare:65 | ||||
| chr3:125595252-125595725 | Common:3; Rare:138 | ||||
| chr3:126084103-126084223 | Common:1; Rare:53 | ||||
| chr3:126180480-126180759 | Common:1; Rare:65 |