| Coordinate | Validation | Epigenomic status | Core promoter element(s) | Mutation | TF registry |
|---|---|---|---|---|---|
| chr3:122564172-122564412 | Common:4; Rare:62 | ||||
| chr3:123201820-123201943 | Common:1; Rare:41 | ||||
| chr3:125520169-125520288 | Rare:34 | ||||
| chr3:126083990-126084178 | Common:2; Rare:54 | ||||
| chr3:127590706-127590911 | Common:2; Rare:44 | ||||
| chr3:127598223-127598417 | Common:3; Rare:46 | ||||
| chr3:127823133-127823271 | Common:1; Rare:26 | ||||
| chr3:128052159-128052473 | Common:2; Rare:105 | ||||
| chr3:128067122-128067446 | Rare:70 | ||||
| chr3:128879429-128879663 | Common:4; Rare:112; Clinvar:2; Clinvar (benign):2 | ||||
| chr3:129183810-129184069 | Common:2; Rare:87 | ||||
| chr3:129316283-129316302 | Rare:10 | ||||
| chr3:129439846-129440333 | Common:1; Rare:150; Clinvar:2; Clinvar (benign):1 | ||||
| chr3:131381513-131381802 | Common:2; Rare:69 | ||||
| chr3:131502870-131503044 | Common:1; Rare:66 |