| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122793788-122793985 | Common:2; Rare:44 | ||||
| chr3:123585028-123585284 | Common:1; Rare:81 | ||||
| chr3:124730340-124730468 | Common:3; Rare:69; Clinvar:1; Clinvar (benign):3 | ||||
| chr3:125375236-125375391 | Rare:42 | ||||
| chr3:125595385-125595704 | Common:1; Rare:88 | ||||
| chr3:127598223-127598438 | Common:3; Rare:55 | ||||
| chr3:128052139-128052500 | Common:4; Rare:120 | ||||
| chr3:128153365-128153493 | Rare:35 | ||||
| chr3:128879408-128879675 | Common:4; Rare:129; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129161013-129161150 | Common:1; Rare:54 | ||||
| chr3:129183814-129184079 | Common:2; Rare:89 | ||||
| chr3:129439843-129440168 | Common:1; Rare:100; Clinvar:1; Clinvar (benign):1 | ||||
| chr3:130893919-130894231 | Common:3; Rare:91 | ||||
| chr3:131381531-131381837 | Common:2; Rare:83 | ||||
| chr3:131502809-131502995 | Common:1; Rare:89 |